Amino-Functional Compounds as Builder/Dispersants in Detergent Compositions

The present invention relates to compounds which can be used as builders, combined builder/dispersants and/or dispersants in detergent compositions. The compounds herein are particularly useful in liquid and granular heavy-duty laundry compositions.

Compositions useful as builders, dispersants or sequestrants are well-known in the art and have widely ranging chemical compositions. See, for example, Berth et al, Angew. Chem. Internat. Edit., Vol. 14, 1975, pages 94-102. Users of commercially available detergents recognize the utility of such materials in the laundry. It is difficult and somewhat arbitrary to categorize the useful compounds by names such as "builder", "dispersant" or "sequestrant", since many art-disclosed compounds have varying combinations of these useful properties, and are widely used in commerce for many purposes, including boiler scale control and water-softening. Nonetheless, experts in the art recognize that such terms reflect real differences in the properties of the compounds; certain compounds, for example, being distinctly better when used at high levels in a builder function, and others, such as polyacrylates, being better in a low-usage role of dispersant. See, for example, P. Zini, "The Use of Acrylic Based Homo- and Copolymers as Detergent Additives", Seifen-Ole-Fette-Wachse, Vol. 113, 1987, pages 45-48 and 187-189. The search for economical new materials having desirable combinations of such attributes thus continues, and the most effective test of their utility is in the simple operation of laundering fabrics.

Recent disclosures of interest include that of U.S. Pat. No. 4,021,359, Schwab, issued May 3, 1977 and U.S. Pat. No. 4,680,339, Fong, issued Jul. 14, 1987. See also Abe et al, Yukagaku 35(11): 937-944, 1986 and Tanchuk et al, Ukr. Khim. Zh. (Russ. Ed.), 43(7), 1977, pages 733-8. See in addition Picciola et al, ".alpha.- and .beta.-Amides of N-Alkyl-and Aralkyl-D,L-Aspartic Acids", Il Farmaco 24 (11), 1969, pages 938-945; Laliberte et al, "Improved Synthesis of N-Alkyl-Aspartic Acids", Can. J. Chem., 40, (1962), pages 163-165; and Zilkha et al, "Synthesis of N-Alkyl-aspartic Acids and N.sup.2 -Alkyl-.alpha.- asparagines", J. Org. Chem., 24 (1959), pages 1096-1098. Schwab discloses compounds comprising water-soluble salts of partial esters of maleic anhydride and polyhydric alcohols containing at least three hydroxy groups, which sequester and retard the precipitation of calcium ions and function as detergent builders. Fong reveals a process for the synthesis of water-soluble carboxylated polymers having randomly repeated amide polymer units. Tanchuk et al disclose certain monoesters of N-(.beta.-hydroxyethyl) aspartic acid, derived by reacting butenedioate monoester with ethanolamine.

Abe et al disclose variants of polymalic acid prepared by ring-opening polymerization of benzyl malolactonate and by direct polymerization of DL-malic acid in dimethylsulfoxide. The detergent builder utility of polymalic acid and biodegradability test results are also disclosed.

The chemistry of maleic anhydride has been comprehensively reviewed. See "Maleic Anhydride", B. C. Trivedi and B. M. Culbertson, Plenum Press, New York, 1982, incorporated herein by reference. Desirably for the large-scale manufacture of laundry detergent chemicals, this compound is available in quantity. Trivedi and Culbertson and the above-referenced Schwab patent make it clear that the reactions of maleic anhydride with alcohols are known in the art. However, the further functionalization of such compounds in the manner of the present invention is apparently unexplored.

As can be seen from the foregoing and as is well-known from the extensive literature relating to laundry detergents, there is a continuing search for improved builders and dispersants. In particular, it would be advantageous to have builders and/or dispersants which can be prepared from readily-available reactants which are biodegradable.

The present invention provides a new class of builder/dispersant materials which help fulfill these needs.

The present invention encompasses compounds of the formula (MAO).sub.n E wherein: n is an integer from 1 to about 2,500; M is H or a salt-forming cation (preferably sodium); A is selected from the group consisting of 2-(sec-substituted-amino)-4-oxobutanoate, 2-(tert-substituted-amino)-4-oxobutanoate, 3-(sec-substituted-amino)-4-oxobutanoate and 3-(tert-substituted-amino)-4-oxobutanoate. O is oxygen covalently bonded to E; and E is a particular organic moiety, defined in detail hereinafter.

The terms "sec-substituted-amino" and "tert-substituted-amino" are here used to emphasize that the oxobutanoate derivatives encompassed contain secondary or tertiary amino groups / moieties and generally exclude oxobutanoates substituted by primary amino groups, i.e., H.sub.2 N-. Compounds of the invention are thus substituted aminooxobutanoates and not H.sub.2 N-substituted oxobutanoates.

A preferred category of materials provided herein encompasses compounds or isomeric mixtures of compounds wherein the A moiety is selected from .crclbar.OC(O)C(L)HCH.sub.2 (O)C-, .crclbar.OC(O)CH.sub.2 C(L)H(O)C- and mixtures thereof, wherein L is a moiety comprising a single secondary or tertiary amino group, provided that when L is ethanolamino, n is greater than 1.

More generally, A moieties can have either of the isomeric formulae ##STR1## wherein the four carbon atoms of the oxobutanoate chain are numbered as shown and wherein an amino-nitrogen atom of a moiety L, now containing one or more secondary or tertiary amino groups, forms a nitrogen-carbon bond to the carbon atom C.sup.2 or C.sup.3.

In the isomer formulae of A, Z is typically hydrogen, hydrocarbyl or another neutral, chemically unreactive group, essential only for the purpose of completing the valencies. Preferably, as noted, Z is H and the A moieties are 2-L-substituted moieties of formula ##STR2##

As indicated in further detail hereinafter, isomeric mixtures of compounds having a major proportion of these preferred C.sup.2 -L, C.sup.3 -H substituted A moieties and a minor proportion of C.sup.2 -H, C.sup.3 -L substituted A moieties, are also effective for the purposes of the invention and can be used, as directly prepared, as dispersants or builders.

In accordance with the above-given definition of A moieties, when M is a monovalent cation, the formula (MAO).sub.n E can be expanded for the purposes of visualizing the general structure as follows for the 2-isomer: ##STR3## and as follows for the 3- isomer: ##STR4##

In general, E can be a monomeric or polymeric moiety having molecular weight in the range from about 15 to about 170,000. The moiety E can be charged or non-charged. When charged, E is typically anionic and can be associated with salt-forming cations such as sodium, potassium, tetraalkylammonium or the like. In general, E can include one or more hetero- atoms such as S (sulfur) or N (nitrogen). Preferably, however, E is a noncharged moiety consisting essentially of C and H, or of C, H and O.

In general, the moiety E has n sites for the covalent attachment, by means of n ester linkages, of said moieties (MAO).sub.n. Thus, each of n ester linkages in any compound (MAO).sub.n E is formed by the connection to E of a moiety MA by means of said oxygen covalently bonded to E.

Preferred compounds (MAO).sub.n E for dispersant applications have molecular weight of E in the range from about 200 to about 15,000; for builder applications, the moiety E is in a molecular weight range from about 15 to about 15,000. Particularly useful compounds herein are those wherein said moiety A has the formula .crclbar.OC(O)C(L)HCH.sub.2 (O)C-wherein L is selected from the group consisting of aspartate, glutamate, glycinate, ethanolamino, .beta.-alanate, taurine, aminoethyl sulfate, alanate, sarcosinate, N-methylethanolamino, iminodiacetate, 6-aminohexanoate, N-methylaspartate and diethanolamino (see structures L.sup.1-14 hereinafter). L is preferably aspartate, glutamate, sarcosinate, glycinate or ethanolamino, and is most preferably aspartate or glutamate.

Preferred E moieties are selected from hydrocarbyl, hydrocarbyloxy, poly(hydrocarbyl) or poly(hydrocarbyloxy) moieties and mixtures thereof in the above-noted preferred molecular weight ranges. Structurally, the preferred E moieties are further characterized in that they can be derived by complete or partial dehydroxylation of alcohols, such as those of formula EOH; to cite a simple example, if EOH is methanol, E is structurally characterized in that it is a methyl group. E is veritably the dehydroxylation product of an alcohol in a structural sense as noted, rather than in a preparative sense. Preparatively and in a mechanistic sense, esterification reactions rather than dehydroxylation reactions are more usually involved in making compounds of the invention. Thus, definition of E in structural terms is not associated with any specific process for making the compounds.

Suitable alcohols for the provision of said moiety E include compounds selected from the group consisting of polyvinyl alcohol, sorbitol, pentaerythritol, starches, glycols such as ethylene and propylene glycol, alcohols such as methanol, ethanol, propanol and butanol. However, E can also be derived from various other linear or branched polyol materials such as sucrose, oligosaccharides, .beta.-methyl glucoside, and glycols such as C.sub.2 -C.sub.6 alkylene glycols.

Typically, suitable alcohols are of types widely available in commerce. A somewhat more uncommon alcohol of the oligosaccharide type is available as M-138, "malto oligosaccharide mixture", Pfanstiehl Laboratories Inc. Suitable oligosaccharide variants could be prepared from cornstarch.

In general, the lower molecular weight materials herein are especially adapted for use as detergent builders. For example, compounds of this invention wherein n is 1 and E is selected from the group consisting of methyl, ethyl, propyl, butyl, ethylene, diethylene, propylene, butylene and hexylene, provide a detergent builder function.

In general, the higher molecular weight (n greater than 1, typically about 4 to about 2,500) materials herein are especially adapted as dispersants or are capable of acting both as dispersants and as builders for use in detergent compositions.

An especially preferred dispersant/builder compound herein is a random copolymer comprising essential repeat units ##STR5## wherein M is sodium, A is .crclbar.OC(O)C(L)HCH.sub.2 (O)C- and L is aspartate. Optional repeat units may also be present. Preferred optional repeat units are selected from ##STR6## and mixtures thereof. Typically, the random copolymer comprises from about 0.10 to about 0.95 mole fraction of the essential repeat units ##STR7## and has a molecular weight in the range from about 635 to about 50,000.

The invention also encompasses processes for making the compounds. For example, the preferred random copolymer illustrated above is readily secured by (i) reacting excess maleic anhydride with a hydrolyzed polyvinyl acetate having average degree of polymerization of about 10 to about 1,500, more preferably about 15 to about 150. Preferably, this polyvinyl acetate is prehydrolyzed to polyvinyl alcohol to a high degree; on a mole percentage basis, the degree of hydrolysis is most preferably in the range from about 70 mole % to about 95 mole %.

The product of step (i) is a butenedioate half-ester, which is (ii) reacted with aspartic acid in an aqueous alkaline medium to form a product which, as noted, is the random copolymer most useful as dispersant/builder in laundry detergent applications. By using a concentrated, buffered alkaline sodium carbonate/bicarbonate reaction medium in step (ii), competing reactions, e.g., hydrolysis, are controlled so that the desired product can be secured in high yield.

The invention also encompasses detergent compositions containing conventional detersive surfactants, bleaches, enzymes, and the like, and typically from about 0.1% to about 35% by weight of the compounds of this invention.

All percentages, ratios and proportions herein are by weight, unless otherwise specified.

The invention encompasses simple, low molecular weight compounds such as ##STR8##

In the simplest compounds, E is an alkyl, alkyloxyalkylene, or alkyl(polyoxyalkylene) group; examples include methyl, ethyl, propyl, butyl, or a group such as CH.sub.3 OCH.sub.2 CH.sub.2 --.

In general, the L group may be attached to either of C.sup.2 or C.sup.3, thus forming an isomeric mixture of compounds of structure Ia and Ib. Typically, in such mixtures, the greater proportion (e.g., about 80 mole percent) of the L groups is attached to C.sup.2 as depicted in Ia, the balance being attached to C.sup.3, structure Ib, to the extent of from about 0 to about 20 mole percent. In structures hereinafter, after, such as II-IX and XI-XVI, the labels ' and * will be used to show the two alternative positions for L substitution; the preferred or major 2-isomer structure, analogous to Ia, is depicted and the minor isomer can be visualized as analogous to Ib.

Suitable groups L herein are typically selected from the following: ##STR9##

Any of the foregoing groups L.sup.1 -L.sup.14 can be used in structures Ia and Ib.

When E is a polyol derivative, the formula is more complex, in that more than one of the above illustrated sec-substituted- or tert-substituted- amino moieties L can be attached to the E substrate; for example, in the builder: ##STR10##

In the above, E is illustrated by the moiety CH.sub.2 CH.sub.2 and, using the general formula (MAO).sub.n E given hereinabove, n is 2. In another illustration, when the E moieties result from a pentaerythritol-like structure, compounds of the invention have the formula ##STR11##

Compositions of the invention can also be prepared by partial substitution of pentaerythritol; which comprise a mixture of compounds (III) together with compounds of formulae: ##STR12##

Compositions of the invention can likewise be prepared in which methylenehydroxy groups partially replace groups attached to the quaternary carbon in any of (III), (IV), (V) and (VI). The novel component of any such composition can thus be represented by the general formula VII which encompasses structures (III) through (VI) as well as methylenehydroxy-substituted variants: ##STR13## wherein a is 0, 1, 2, or 3; b is 0, 1, 2, or 3; c is 1, 2, 3 or 4, and a+b+c=4.

Another typical compound herein includes an E moiety having a sorbitol-like structure; this compound can be represented by the formula (Fisher projection): ##STR14##

E can also be derived from a cyclic polyol; thus, compounds of the invention can, for example, be M.sym.A.crclbar.-substituted .alpha.- or .beta.-methyl glucoside derivatives; one representative .alpha.-derivative has the formula: ##STR15##

As in the above-given structures (IV) through (VII), novel compounds having proportions of (OH) groups or butenedioate half-ester, i.e., (--C(O)CHCHCO.sub.2 .crclbar.Na.sym.) groups replacing AM groups can be present in compositions containing the compounds of formulas (VIII) or (X), especially if compounds (VIII) or (X) are not used in chemically purified form.

When E is a simple homopolymer-type group, compounds of the invention are oligomeric or polymeric; for example, a homopolymer based on polyvinyl alcohol fully substituted by groups of structure (IX) is represented by: ##STR16##

The end-groups of the homopolymer in this instance will be the usual PVA end-groups, dependent upon well-known initiators and terminators used in PVA synthesis.

Co-oligomers or copolymers having the essential (MAO) units can also be prepared. These may be simple copolymers, or may be terpolymers, tetrapolymers or the like. Random polymers according to the invention typically contain, by way of essential units, units of the formula (XI); a particular copolymer of interest herein is represented by the units ##STR17## wherein both head-to-tail and tail-to-head arrangements of the a and b units occur.

Also encompassed herein are random oligomers or polymers represented by formulas such as (XIII)-(XV). ##STR18##

A more complex oligomer or polymer can be derived by bisulfite addition across a proportion of the c- units in (XIV), yielding ##STR19## in which instance addition of sulfate will favor the carbon atom at the C** position.

In (XIII)-(XV), the (a) essential repeat units are complemented by the optional units having subscripts (b)-(e). C" and C** are defined in a manner analogous to C' and C*; thus sulfonation at C** is preferred.

A preferred polymeric compound of the invention having mer- units containing amino-, alcohol and acetate moieties is represented by the formula ##STR20## Head-to-tail and tail-to-head arrangements of the units are included. Units (a+b+d) together typically sum to a value of about 100. In one preferred embodiment, a is 60 or higher, b is about 25 and d is about 15.

In all of the foregoing formulas, sodium cations can be replaced by other cations, especially H.sup.+ or other water-soluble cations such as potassium, ammonium and the like.

Additional detail surrounding preferred embodiments of the instant invention is as follows:

As noted supra, it is clearly preferred herein to make use of an oligomeric or polymeric moiety E which is substantially noncharged. The term specifically excludes from E any highly charged polyanion moieties such as polyacrylate derivatives, in contrast with the desirable polyol derivatives such as are illustrated herein.

The situation pertaining to charge of moieties L has been discovered to differ from that pertaining to moieties E. Thus, it is preferred herein to select charged L moieties such as L.sup.1 -L.sup.3, L.sup.5 -L.sup.9 and L.sup.11 -L.sup.13 (see structures supra), as distinct from L.sup.4, L.sup.10 and L.sup.14.

In consequence, a selected group of compounds particularly useful for the provision of laundry detergent builders and dispersants encompasses compounds of the formula (MAO).sub.n E wherein n is an integer from 1 to about 2,500, M is H or a salt-forming cation; A is selected from the group consisting of: 2-(sec-substituted-amino)-4-oxobutanoate of the formula .crclbar.OC(O)C(L)HCH.sub.2 (O)C- wherein L is a sec-amino moiety, 2-(tert-substituted-amino)-4-oxobutanoate of the formula .crclbar.OC(O)C(L)HCH.sub.2 (O)C- wherein L is a tert-amino moiety, 3-(sec-substituted-amino)-4-oxobutanoate of the formula .crclbar.OC(O)CH.sub.2 C(L)H(O)C- wherein L is a sec-amino moiety, 3-(tert-substituted-amino)-4-oxobutanoate of the formula .crclbar.OC(O)CH.sub.2 C(L)H(O)C- wherein L is a tert-amino moiety, and mixtures thereof; and E is a substantially noncharged moiety having molecular weight in the range from about 15 to about 170,000; wherein said moiety E has n sites for the covalent attachment of said moieties (MAO).sub.n ; wherein said moiety E consists essentially of C and H or of C, H and O; and wherein, when said moiety L is a sec-amino moiety, L is selected from the group consisting of aspartate, glutamate, glycinate, beta-alanate, taurine, aminoethylsulfate, alanate and 6-aminohexanoate; and when said moiety L is a tert-amino moiety, L is selected from the group consisting of sarcosinate, iminodiacetate and N-methylaspartate.

It is desirable, especially for the provision of dispersants, to have one, preferably a plurality of covalently bonded oxygen atoms present within E, and to use inexpensive, safe, and water-soluble salt-forming cations such as those of sodium or potassium. Thus, the invention identifies useful compounds wherein said salt-forming cation M is a water-soluble cation, said moiety A has the formula .crclbar.OC(O)C(L)HCH.sub.2 (O)C-, and said moiety E consists essentially of C, H and O and has a molecular weight in the range from about 45 to about 15,000. The lower limit of molecular weight of E in these compounds is consistent with the presence of at least one oxygen atom.

In dispersant applications, it is highly desirable to have a plurality of charged moieties MAO. Thus, n will preferably be greater than 1; more preferably, at least 3 moieties MAO will be present for each moiety E. For best results as a dispersant, however, n will preferably not exceed about 250. Thus, the invention encompasses compounds wherein M is sodium; n is from about 3 to about 250 and said moiety E has a molecular weight in the range from about 45 to about 15,000 and is structurally characterized in that it comprises the fully or partially dehydroxylated product of a dihydric or polyhydric alcohol.

Preferred dihydric or polyhydric alcohols suitable for use herein can, in general terms, be described as those selected from the group consisting of:

(i) polyvinyl alcohol;

(ii) pentaerythritol;

(iii) saccharide selected from mono-, di-, oligo and polysaccharides;

(iv) glucoside selected from alcohol glucosides and glycol glucosides;

(v) alkylene glycol selected from C.sub.2 -C.sub.6 alkylene glycols;

(vi) sorbitol and

(vii) mixtures thereof.

Suitable saccharides are illustrated by maltose, lactose, sucrose, malto-oligosaccharide and starch.

Suitable glucosides are illustrated by .alpha.-methylglucoside, ethylene glycol glucoside and propylene glycol glucoside.

As associated with polyvinylalcohols used for the provision of E, especially in the context of dispersant compounds, the practitioner will recognize the term "degree of hydrolysis" in its conventional sense. More specifically, whether the polyvinylalcohol has actually been made from polyvinylacetate by methanolysis or not, "degree of hydrolysis" is a useful term quantifying the essential --OH group content as distinct from the content of nonhydrolyzed groups such as acetate, which may be optionally be present. The term is used by suppliers of polyvinylalcohol. Most highly preferred polyvinylalcohol samples for use herein have a degree of hydrolysis of 70% or higher. The corresponding compounds, especially adapted for use as a dispersant or dispersant/builder for use in detergent compositions, are those wherein the structure of moiety E corresponds with its derivation from an alcohol which is, specifically, polyvinyl alcohol characterized by a degree of hydrolysis of about 70% or higher.

The practitioner will naturally recognize that polyvinylalcohol having a degree of hydrolysis of less than 100% will generally have random or blocky copolymer distribution of the vinyl alcohol and vinyl acetate mer-units. When incorporated into a compound of the invention, the polymer structure of the compound as a whole will naturally be influenced by this distribution.

In a preferred embodiment, compounds herein which are derived from polyvinylalcohol thus consist essentially of a random copolymer. This random copolymer preferably has a molecular weight in the range from about 635 to about 50,000, even more preferably about 4950 to about 49,500, the molecular weight of the compound as a whole being determined by the molecular weight of the polyvinyl alcohol used as well as by the relative proportion, i.e., mole fraction, of moiety A. Preferably, the compound is a random copolymer containing about 0.10 to about 0.95 mole fraction, even more preferably about 0.60 to about 0.95 mole fraction, of repeat units of the formula ##STR21## wherein M is sodium and A is .crclbar.OC(O)C(L)HCH.sub.2 (O)C-. L is a charged moiety in accordance with the definition supra, and is preferably selected from the group consisting of aspartate, glutamate, glycinate, taurine, sarcosinate and iminodiacetate.

In process terms, such compounds can be produced by reacting said polyvinylalcohol together with maleic anhydride and an amine reactant selected from aspartic acid, glutamic acid, glycine, taurine, sarcosine, iminodiacetic acid or water-soluble salts thereof.

Most preferably, the process is rather specific, and involves the following sequence of steps:

(i) reacting said polyvinyl alcohol with maleic anhydride to produce a butenedioate half-ester of said polyvinyl alcohol; and

(ii) reacting said butenedioate half-ester with said amine reactant.

In these process steps, it is important to note that step (ii) is conducted in an aqueous medium and the alkalinity is controlled by means of a carbonate-buffer, as further illustrated hereinafter.

One very effective method for carrying out step (i) involves reacting a mixture formed from said polyvinyl-alcohol and maleic anhydride together with tetrahydrofuran as solvent and an effective amount of an acetate catalyst; provided that said mixture comprises in total no more than from about 5% to about 20% tetrahydrofuran. This produces a butenedioate half-ester of said polyvinyl alcohol; which is purified to complete step (i), by partitioning into the lower layer of a tetrahydrofuran/water mixture, said mixture having a volume/volume ratio of said tetrahydrofuran and water ranging from about 1/2 to about 1/12.

In more detail, the compounds of the invention are generally prepared by a two-part procedure. The first step of this procedure generally involves reacting maleic anhydride with compounds which contain hydroxyl groups so as to form butenedioate half-esters. Typical of such hydroxyl-containing compounds (alcohols) are polyvinyl alcohol, pentaerythritol, tripentaerythritol, sorbitol, 1,3-propanediol, and, less desirably, ethanol, isopropanol, n-butanol and methanol.

It is especially preferred to use an alcohol identified as belonging to one of the categories (i)-(vii) supra.

The step 1 reaction can be conducted with or without a catalyst; generally a basic catalyst such as sodium carbonate or sodium acetate is used. A solvent for the reaction is not generally necessary since the compound containing the hydroxyl group is typically either soluble in maleic anhydride or swelled by maleic anhydride. When a solvent is used, one suitable for swelling or solubilizing the hydroxyl-containing compound is selected; solvents such as tetrahydrofuran, dioxane and dimethylformamide are satisfactory.

The choice of reaction temperature for step 1 depends on the steric environment of the hydroxyl groups; esterification of secondary alcohols usually requires a higher reaction temperature than esterification of primary alcohols. Generally a reaction run in THF at reflux (approximately 65.degree. C.) is sufficient to esterify most primary and secondary hydroxyl groups. Reactions run without solvent require higher temperatures, usually between about 80.degree. C. and about 120.degree. C. to achieve the same extent of esterification as reactions run with solvent.

The amount of maleic anhydride required for the reaction is selected in dependence of

(a) whether the hydroxyls are primary or secondary;

(b) the degree of esterification desired; and

(c) whether a solvent is to be used. If the hydroxyl groups are primary, a 1:1 molar ratio of hydroxyl groups to maleic anhydride will typically result in esterification of more than 60 mole percent of the hydroxyl groups, provided that a solvent is used and that a temperature of 65.degree. C. or above is employed. Under the same reaction conditions, secondary alcohols may require as much as a 2:1 molar excess of maleic anhydride to hydroxyl groups in order to achieve a similar degree of esterification. When lesser degrees of esterification are desired, a molar deficiency of maleic anhydride to hydroxyl groups may be employed, and a solvent will generally be used in the reaction.

When the reaction is conducted without solvent, a molar excess of maleic anhydride to hydroxyl groups is normally required so that the resulting reaction mixture is fluid.

When using a solvent, the amount employed is usually the minimum necessary to achieve swelling or solubilization of the hydroxyl-containing compound; typically, solvent comprises about 5% to 60%, more preferably from about 5% to about 20% by weight of the reaction mixture. Unexpectedly, use of low levels of solvent generally leads to improved esterification yields.

When the hydroxyl-containing compound is highly swelled by the solvent, the order of reactant addition can be important. Thus, it is often preferable to have the maleic anhydride and catalyst dissolved in the solvent first, and to heat this solution to 50.degree. C. The hydroxyl-containing compound is then added. The hydroxyl-containing compound partially esterifies during the addition, preventing the viscosity from becoming excessively high.

The step 1 reaction herein and the product thereof are typically represented by: ##STR22## wherein XVII is a typical butenedioate half-ester which can contain cis- or trans- configurations of the double bond between C' and C*. Up to 80% or more of the mer-units can be functionalized; e.g., in XVII n' and n" are, respectively 0.8 X or more and 0.2 X or less as fractions of the overall degree of polymerization. Other mer-units, such as those derived from vinyl acetate, e.g., ##STR23## can commonly be present. The first synthesis step herein is further illustrated by nonlimiting Examples I-V hereinafter.

The following patents and patent documents, all incorporated herein by reference, further illustrate the first step used in preparing compounds of the invention. The compounds described in these references are generally suitable herein as butenedioate half-ester starting compounds for the step 2 reaction described hereinafter: U.S. Pat. No. 4,021,359, Schwab, issued May 3, 1977; Russian Journal Article Vysokomol. Soedin., Ser. B., 1976, Vol 18 (11), pages 856-8, Korshak et al; and Japanese patent documents JP 85/1480, assigned to Nippon Shokubai, published Jan. 10, 1985; JP 79/20093, Yoshitake, published September 13, 1979; JP 77/85353, assigned to Kuraray KK, published Jul. 15, 1977; JP 78/52443, assigned to Kuraray KK, published Apr. 28, 1978; JP 84/36331, assigned to Nippon Oils and Fats KK, published Feb. 29, 1984; Jp 78/27119, assigned to Kuraray KK, published Mar. 7, 1978; JP 77/59083, assigned to Kuraray KK, published May 20, 1977; JP 77/94481, assigned to Kuraray KK, published Aug. 5, 1977 and JP 77/94482, assigned to Kuraray KK, published Aug. 5, 1977.

By reacting the butenedioate half-esters of the first step using a particular second step (itself part of the invention), the compounds of the invention are readily secured.

The second step of the synthesis of compounds of the invention presents a significant technical challenge. If the above-described half-esters are to be reacted with particularly defined amines or amino acids (these amine reactants are generally of a water-soluble type; see reaction (i) below), it is necessary to use an aqueous solvent system for the reaction because of the low solubility of the amine or amino-acid in common organic solvents. However, use of an aqueous solvent system inherently introduces competing reactions, such as ester hydrolysis of the butenedioate half-ester reactant or of the 2-amino-4-oxobutanoate product. ##STR24##

The process of the present invention overcomes the ester hydrolysis problem and allows the step 2 reaction (i) to proceed smoothly with minimized reverse reaction (ii) to provide 2-amino-4-oxobutanoate compounds as noted, in high yield.

Reactants used are typically

(a) a particularly defined amine or amino-acid of formulas L.sup.1 H through L.sup.14 H;

(b) sodium hydroxide (preferably as an aqueous solution);

(c) water (solvent);

(d) butenedioate half-ester of step 1; and

(e) sodium carbonate.

The procedure typically involves

(i) comixing (a), (b) and (c);

(ii) cooling the mixture, typically to 0.degree.-10.degree. C.;

(iii) adding (d);

(iv) progressively warming, to a temperature not in excess of about 100.degree. C., more typically up to about 80.degree. C., preferably not in excess of about 65.degree. C., so that (d) disperses or dissolves;

(v) adjusting the temperature to below about 50.degree. C.;

(vi) adding (e); and

(vii) reacting the reaction mixture at a temperature ("reaction temperature") generally above ambient temperature, typically about 20.degree. C. to about 80.degree. C. depending upon a temperature-alkalinity relationship further detailed hereinafter, to form the product. (Reaction times are typically about 1 to about 24 hours.)

In the above, the amounts of (a) and (d) are selected according to stoichiometry. Compounds of the invention derived by this procedure may be used as directly prepared or may be further purified, prior to use in detergent compositions.

In general, the reactant (a) in the above procedure is a water-dispersible or soluble amine or amino acid, which has at least one amino group which when protonated, has a pK.sub.a less than about 11. This amino group is necessarily primary or secondary (since it is used for making a sec- or tert- product of step 2 respectively) and is not subject to significant steric hindrance. Amines or amino-acids having some degree of steric hindrance can be used, provided that the reactions proceed at a reasonable rate. In general, the term amino-acid encompasses aminocarboxylic acids, aminosulfuric acids and aminosulfonic acids.

In general, when the reactant (a) is not an amine but is an amino-acid derivative, reactant (a) can be used as a fully or partially neutralized water-soluble cation salt. To illustrate, suitable variants of a preferred reactant (a) based upon the group L.sup.7 illustrated hereinabove include the salt L.sup.7 H, i.e., aminoethylsulfuric acid sodium salt, and free aminoethylsulfuric acid. For convenience, such reactant is simply identified as "aminoethylsulfate". Other preferred reactants (a) are sodium salts of formulae L.sup.1 H through L.sup.6 H and L.sup.8 H through L.sup.14 H, together with their corresponding free acids.

In addition to the reactant selection, order of addition and temperature control, all as noted, the following are found to be especially important parameters to secure compounds of the invention in good yield from the step 2 reaction:

(i) alkalinity;

(ii) buffering; and

(iii) water content.

In the above, control of alkalinity is most important; specific buffering provides the means for alkalinity control, and control of water content is highly desirable.

The step 2 reaction uses generally high alkalinity. pH is not an exact measure at the high concentrations used, but as a guideline, alkalinity is typically greater than or equal to pH of about 10. However, high alkalinity alone can result in ester hydrolysis as noted.

Thus, to prevent hydrolysis in the alkaline reaction mixture, a combined NaOH/Na.sub.2 CO.sub.3 alkalinity/buffering system is used. (It will be appreciated that in the presence of acidic organic reactants, a carbonate-bicarbonate buffer system is set up, i.e., the inorganic salts present in situ comprise NaOH, Na.sub.2 CO.sub.3 and NaHCO.sub.3). In the simple case of reacting an amine such as ethanolamine (1 mole) with a butenedioic acid half-ester (1 mole), about 0.1 mole of NaOH followed by about 0.5 moles Na.sub.2 CO.sub.3 are used. Thus, the NaOH/Na.sub.2 CO.sub.3 amount in total is calculated to fully neutralize the acid and provide an excess of alkalinity to enable the forward reaction. When the amine itself is an .alpha.-amino acid, e.g., aspartic acid (1 mole), about 2.6 moles of NaOH and about 0.5 moles of Na.sub.2 CO.sub.3 are used. Together, these amounts are calculated to fully neutralize the butenedioic portion of the acid present, neutralize the 2 moles of H.sup.+ present in the aspartic acid and provide 0.6 moles excess base. The relatively large amount of excess base is needed because of the high pK.sub.a of the aspartate ammonium group (.about.9.7 compared with only .about.9.0 for the ethanolamine ammonium group). In the case of .beta.-amino acids (1 mole), the amounts of NaOH (1.1 mole) and Na.sub.2 CO.sub.3 (0.5 moles) are calculated analogously by those of the ethanolamine illustration hereinabove, but also take into account the amino acid carboxylate groups. Clearly, this procedure suggests that it is appropriate to select the proportions of NaOH/Na.sub.2 CO.sub.3 in general, in accordance with the pK.sub.a 's of ammonium groups of the amines and in accordance with the number of moles acidic carboxylate added in total from both possible sources (butenedioic half-ester and acidic amino carboxylate).

In general, it is also possible to use alternative buffer systems provided that they effectively buffer in a pH region similar to the hydroxide/carbonate/bicarbonate system illustrated.

The step 2 reaction also uses high aqueous concentrations of reactants (a) and (d). Taking these components together, calculated as the sodium salts, weight concentrations in the range from about 30% to about 60%, more preferably from about 40% to about 55% of the reaction mixture are typically used.

The step 2 reaction further appears to have a combined alkalinity-temperature relationship which, for best results, needs to be optimized. Thus, higher alkalinity and lower temperatures work effectively together; conversely lower alkalinity together with higher reaction temperatures provide a second set of optimum reaction conditions. The lower reaction temperature optimum and higher reaction temperature optimum are illustrated as follows for the aspartic acid system described:

While not intending to be limited by theory, it is foreseeable that for each of the amines L.sup.1-14 H herein, similar optima will exist. These are readily identified within the typical range of temperature and NaOH/Na.sub.2 CO.sub.3 usage specified herein.

1A. Product of Reacting Maleic Anhydride with --OH Reactant Alcohols--To a weighed 500 mL three-neck round bottom flask fitted with a mechanical stirrer, condenser, and gas outlet are added tetrahydrofuran (20 ml), maleic anhydride (68.99 g, 0.704 mol), and sodium acetate (0.0288 g, 0.000352 mol). The reaction mixture is heated under argon in an oil bath held at 50.degree. C. The --OH reactant (in an amount sufficient to provide 0.352 mol of hydroxyl groups) is added over 5 minutes to the reaction mixture, with rapid stirring. The oil bath temperature is then raised to 65.degree. C.; the reaction mixture is maintained at about this temperature for about 6 to about 42 hours to give a clear solution of product. The extent of esterification is determined using Procedure 1C, then solvent is stripped from the reaction mixture to provide a solid, gummy product.

1B. Purification, optionally, can be carried out as follows. This procedure is especially applicable when the --OH reactant is polyvinyl alcohol.

Excess maleic anhydride is removed from the product of Procedure 1A (as directly prepared) by dissolving the product of Procedure 1A in tetrahydrofuran (100 ml) with stirring and then pouring the resulting solution into three times its volume of water. Most generally, the tetrahydrofuran/water volume/volume ratio is from about 1/2 to about 1/12. This yields a two-phase liquid mixture. The desired product is in the lower layer or phase, leaving excess or free maleic acid in the upper layer or phase. The lower layer is separated and is freeze-dried. Its ester content can be determined by Procedure 1E.

1C. Determination of Butenedioate Half-Ester Content

The sides of the round-bottom flask and condenser from 1A are rinsed with THF to return any sublimed maleic anhydride back to the reaction mixture. The reaction flask and its contents are weighed and the weight of reaction mixture determined by difference. A weighed aliquot (.about.250 mg) of the mixture is removed and titrated with 0.1N sodium hydroxide using phenol red as indicator. Assuming no loss of reactants during the course of the reaction, the butenedioate half-ester content is calculated as: Q.sub.1 =moles butenedioate half-ester per gram of reaction mixture=2 (moles maleic anhydride used per gram of reaction mixture)--(moles residual acid as determined by the titration, expressed per gram of reaction mixture). Since it is known how many moles of hydroxy groups are present in the --OH reactant used in reaction 1A, it is also possible to determine the average degree of esterification of the sample. On a mole percentage basis, the degree of esterification is given by the above-determined amount Q.sub.1 divided by the moles of hydroxy groups present in the --OH reactant used, per gram of reaction mixture.

1D. Determination of Total Acidity of Product of 1A or 1B

An aliquot of product of 1A or 1B is titrated using 0.1N NaOH to a phenol red end-point and the quantity Q.sub.2 =moles acid group per gram of butenedioate half-ester is determined.

1E. Determination of Butenedioate Half-Ester Content of Purified Product of 1A

To a 25 mL one-neck round bottom fitted with a stir bar, condenser and gas outlet is added a weighed (.about.30 mg) aliquot of the half ester product of Procedure 1B. 0.1N sodium hydroxide (10.0 ml, 1.0 mmol) is added. The reaction mixture is heated under argon using an oil bath 100.degree. C. for 30 minutes so as to completely hydrolyze all esters. The reaction mixture is cooled to room temperature and titrated with a 0.1N hydrochloric acid to a phenol red end point. The difference between this titre per gram of reaction mixture and Q.sub.2 (determined in Procedure 1D) gives Q.sub.1 (the molar amount of ester units per gram of purified product of 1A).

Using the above-described procedures, selecting specific --OH reactants according to the following table, the first step of the synthesis is carried out:

2A. Addition of Aminofunctional Reactant (a) to Product of Procedures 1A or 1B at 37.degree. C.

Select an amount Y grams of product of Procedure 1A or 1B, analyzed to determine Q.sub.1 (using procedures 1C or 1E) and Q.sub.2 (using Procedure 1D). The weight taken is selected to provide 0.017 moles of butenedioate half-ester groups. To a 25 mL three-neck round bottom fitted with a gas inlet and means for mechanical stirring are added amine reactant (0.017 mol), water (2.5 g), and an aqueous solution comprising 40% by weight sodium hydroxide. The weight (W) of this 40% NaOH solution is

when the amine reactant selected is aspartic acid,

when the amine reactant selected is sarcosine or glycine, and

when the amine reactant selected is ethanolamine.

The reaction mixture is cooled by placing the flask in an ice bath and the Y gram aliquot of the product of procedure 1A or 1B is added in a single portion with stirring. The reaction flask is heated using an oil bath at 37.degree. C. with vigorous stirring. Typically, a milky suspension is obtained. Then sodium carbonate (0.8079, 0.0085 mol) is added slowly, so as to prevent excessive foam formation. The reaction mixture is kept in the oil bath at 37.degree. C. for 4 hours, cooled to room temperature and then diluted with an equal volume of water. This solution is adjusted to pH 7 with 0.1N sulfuric acid and then freeze-dried to give a white solid. Alternatively, without adjusting pH, purification procedure (see 2C or 2D hereinafter) is used.

Using the above-described Procedure 2A, the products of the first step of the synthesis are used to make compounds of the invention as follows:

To a weighed 500 ml three-neck round bottom flask fitted with stir bar, condenser, and gas outlet are added tetrahydrofuran (125 ml), maleic anhydride (68.99 g, 0.704 mol), and sodium acetate (0.0288 g, 0.000352 mol). The reaction mixture is heated to 50.degree. C. under argon in an oil bath. Polyvinylalcohol (GOHSENOL tradename from Nippon Gohsei, degree of polymerization .perspectiveto.100, 87% hydrolyzed, 20.0 g, 0.352 mol of hydroxyl groups) is slowly added. The oil bath temperature is then raised to 65.degree. C.; the reaction mixture is maintained at about this temperature for 28 hours to give an amber solution. The degree of esterification of the polyvinylalcohol is determined by Procedure 1C to be 79%. Then solvent is stripped from the reaction mixture to provide a solid, gummy product (97.7 g) which is purified as follows.

The gummy product is dissolved with stirring in tetrahydrofuran (100 ml) at room temperature; this solution is poured into vigorously stirred water (500 ml) to give a two-phase liquid. The desired product is in the bottom liquid phase leaving excess or free maleic acid in the top liquid phase. The bottom liquid phase is separated and the tetrahydrofuran stripped off to provide a viscous, beige liquid (68.0 g). This liquid is mixed with water (50 ml) and then freeze-dried to give a beige solid, 42.3 g; .sup.1 HNMR (referenced to 3-{trimethylsilyl}-propionic-2,2,3,3-d.sub.4 acid, sodium salt), .delta.1.3-2.5 (broad multiplet), .delta.4.5-5.4 (broad multiplet), .delta.5.9-6.5 (multiplet). The beige solid is reacted with aspartic acid using the following method:

The beige solid was first analyzed to determine Q.sub.1 and Q.sub.2 using Procedures 1E and 1D, respectively: Q.sub.1 =0.00681 moles butenedioate half-ester groups per gram of solid, Q.sub.2 =0.006876 moles acid groups per gram of solid. The amount of beige solid to provide 0.017 moles of butenedioate half-ester groups can be calculated: ##EQU1##

To a 25 ml three-neck round bottom fitted with a gas inlet and means for mechanical stirring is added aspartic acid (2.27 g, 0.017 mol) deuterium oxide (2.5 g), and an aqueous solution comprising 40% sodium deuteroxide. The weight of NaOD solution is

The reaction mixture is cooled by placing the flask in an ice bath and the 2.5 g aliquot of the beige butenedioic half-ester solid is added in a single portion with stirring.

The reaction flask is heated with stirring using an oil bath at 37.degree. C. Then sodium carbonate (0.900 g, 0.0085 mol) is added slowly, so as to prevent excessive foam formation. The reaction mixture is kept in the oil bath at 37.degree. C. for 4 hours and then diluted with an equal volume of water; the pH of this solution is 9.81.Next the pH of the solution is adjusted to 7.0 using 0.1N sulfuric acid and then freeze-dried to give a white solid (5.8 g). This solid is purified further using gel permeation chromatography as described in Procedure 2D, below.

The white solid (0.92 g) is dissolved in 10 ml of water. This solution is loaded onto a 2.5.times.95 cm column of BIOGEL P2 (BioRad Corp.) or equivalent polyacrylamide gel and eluted at a flow rate of 12-16 ml/hour for about 15.5 hours, and then at 25-35 ml/hour for 8 hours. The desired product elutes in the 250-400 ml volume fraction, the impurities in the 400-470 ml fraction. The 250-400 ml volume fraction is freeze dried to give a white solid: 0.30 g; .sup.1 H NMR (reference to 3-{trimethylsilyl}-propionic acid-2,2,3,3-d.sub.4 acid, sodium salt) .delta.1.3-2.1 (broad multiplet), .delta.2.5-3.1 (broad multiplet), .delta.3.5-4.0 (broad multiplet), .delta.4.7-5.3 (broad multiplet); elemental analysis: C, 38.57%; H, 4.58%; N, 3.32%.

To a weighed 1000 ml three-neck round bottom flask fitted with mechanical stirrer, condenser, and gas outlet are added tetrahydrofuran (170 ml), maleic anhydride (493.8 g, 5.04 mol), and sodium acetate (0.225 g, 0.0027 mol). The mixture is heated under argon in an oil bath to 50.degree. C. until the maleic anhydride dissolves. Polyvinylalcohol (GOHSENOL, Nippon Gohsei, degree of polymerization .congruent.100, 87% hydrolyzed, 150.0 g, 2.63 mol of hydroxyl groups) is added over about 3 minutes. The oil bath temperature is then raised to 65.degree. C.; the reaction mixture is maintained at about this temperature for 25 hours to give an amber viscous solution. The degree of esterification of the polyvinylalcohol is determined by Procedure 1C to be 97%.

The reaction mixture (about 700 ml) is poured with stirring into vigorously stirred water (2000 ml) at 10.degree. C., to give a two-phase liquid. After stirring for 1 hour at 25.degree. C., the phases are allowed to separate. The desired product is in the lower liquid phase, leaving excess or free maleic acid in the upper liquid phase. The lower liquid phase (about 500 ml) is removed and diluted with fresh tetrahydrofuran (800 ml). The resulting solution is poured into fresh water (1400 ml) and stirred vigorously for 1 hour at 25.degree. C. Decantation of the lower liquid phase into four 9".times.15" glass baking pans to a depth of 1 cm is followed by evaporation in the hood for 18 hours. Residual solvent is removed from the gummy material in vacuo for 48 hours at 25.degree. C., producing a rigid, glassy foam. This is then pulverized to an off-white powder (272 g). .sup.1 HNMR (referenced to 3-{ trimethylsilyl}-propionic-2,2,3,3-d.sub.4 -acid, sodium salt), .delta.1.3-2.5 (broad multiplet), .delta.4.5-5.4 (broad multiplet), .delta.5.9-6.5 (multiplet). This solid is reacted with aspartic acid using the following method:

The solid is first analyzed to determine Q.sub.1 and Q.sub.2 using Procedures 1E and 1D, respectively: Q.sub.1 =0.00602 moles butenedioate half-ester groups per gram of solid, Q.sub.2 =0.00595 moles acid groups per gram of solid. The amount of solid to provide 0.244 moles of butenedioate half-ester groups is calculated as ##EQU2##

An aspartate solution is made by dissolving aspartic acid (45.3 g, 0.341 mol), water (50 g), and a 50% w/w solution of sodium hydroxide in water (62.8 g). This solution is cooled to about 0.degree. C. The amount of the sodium hydroxide used is based upon the following calculation: ##EQU3##

To a 500 ml, 3-neck round bottom flask fitted with a gas inlet, mechanical stirrer and two addition funnels are comixed at 0.degree. C., each in a number of about equal portions from its separate addition funnel, the "Y" gram aliquot of butenedioic half-ester solid (40.5 g, 0.244 mol) and simultaneously, aspartate solution (158.1 g) over about 15 minutes. The reaction mixture is mixed with vigorous stirring, to produce a creamy, viscous whip. The reaction vessel is then warmed to about 37.degree. C. in an oil bath. Sodium carbonate (18.0 g, 0.17 mol) is now added slowly, to prevent excessive foam formation. The reaction mixture is kept in the oil bath at 37.degree. C. for 4 hours, is cooled to ambient temperature and is then diluted with an equal volume of water; the pH of this solution is 9.81. The product can now optionally be purified using procedure 2B. If it is desired to use the product without the purification procedure 2B, the pH of the solution is adjusted to 7.0 using 1.0N sulfuric acid and then freeze-dried to give a white solid (136 g). This material can be used without further purification as a random copolymer suitable for use e.g., at levels of from about 0.1% to about 10%, as a dispersant in laundry detergent formulations, as further illustrated hereinafter; such formulations comprise a detersive surfactant and need not comprise any conventional dispersant such as polyacrylate.

2B. Purification of the Product of Procedure 2A:

Polyol-derived crude products can simply be purified by precipitation from aqueous solution. For example, polyvinylalcohol-derived products can be precipitated at a pH of about 2.4.

More generally, contaminants such as maleic acid, fumaric acid, and traces of the starting amine reactant can be removed by pouring the crude product solution (as directly prepared before pH adjustment to 7) into methanol (typically 3 to 6 times by volume). The desired product precipitates enriching the solution with contaminants. However, some quantity of contaminants may still be in the precipitate. This precipitate can be further purified by dissolving it in water to make a 50% by weight solution and then pouring this solution into methanol. The desired product precipitates. This procedure can be repeated several times to further remove impurities from the desired product. 2C. An alternative purification procedure can be carried out using gel permeation chromatography to separate the components of the reaction mixture by molecular weight. The fractionation is carried out at room temperature using a 2.5.times.100 cm ALTEX column; the eluent is monitored by a WATERS Model R403 refractive index detector. Eluent flow is maintained by a MASTER FLEX peristaltic pump. The gel used generally is BIO GEL P-2 (approximately 150 g). The void volume of the column is approximately 150 ml.

Approximately 0.5 g of the product of procedure 2A is dissolved in 5 ml of water. This solution is loaded on a column and eluted at a flow rate of about 12-15 ml/hour. The order that the components elute corresponds to their molecular weight; high molecular weight components elute first, lower molecular weight components elute later. Subsequent to gpc purification, compounds of the invention are characterized in the normal manner by NMR spectroscopy, elemental analysis and the like.

Compounds of the invention are effective dispersants, especially for clay soils, magnesium silicate and calcium pyrophosphate. They may be used at low levels in laundry detergents as dispersants or at higher levels, as laundry detergent builders.

Depending on whether it is desired to use compounds of the invention primarily in a dispersant role or primarily in a builder role, it is possible to incorporate the compounds at a wide range of levels in laundry detergent compositions. Compounds of the invention, as prepared, may thus be directly incorporated into laundry detergents at levels ranging from about 0.1 to about 35%, and higher, by weight of the finished composition. The preferred dispersant applications use levels in the range from about 0.1% to about 6% by weight of the laundry detergent composition while the preferred builder applications typically use levels in the range from about 6% to about 35%.

While it is possible to formulate very simply by use of no more than a single surfactant, preferred laundry detergent compositions herein are more complex. For example, when using the compounds as dispersants, at least one surfactant and at least one conventional detergent builder are typically used, the latter preferably phosphate-free or in the form of pyrophosphate.

Thus, laundry detergent compositions are encompassed such as those comprising a detersive surfactant and one or more conventional, nonpolymeric detergent builders and, as dispersant, from about 0.1% to about 10% of the compound of claim 3. It is especially advantageous that such compositions can be made and used substantially free from polyacrylate dispersant.

In preparing laundry detergent formulations, precautions are generally taken to avoid directly contacting the compounds of the invention with concentrated acids or alkalis, especially when elevated temperatures are used in formulation. Typical laundry detergent formulas for use herein include both phosphate-built and, preferably, phosphate-free built granules, pyrophosphate-containing built granules, phosphate-free built liquids and European-style nil-phosphate granules. See the following patents and patent applications, all incorporated herein by reference.

Compounds of the invention, as prepared, can simply replace at dispersant levels the polyacrylate component of conventionally formulated laundry detergents, or at builder levels, the builder component, with excellent results.

More particularly, the detergent formulator will be assisted by the following disclosure:

Detersive Surfactants: The detergent compositions of this invention will contain organic surface-active agents ("surfactants") to provide the usual cleaning benefits associated with the use of such materials.

Detersive surfactants useful herein include well-known synthetic anionic, nonionic, amphoteric and zwitterionic surfactants. Typical of these are the alkyl benzene sulfonates, alkyl- and alkylether sulfates, paraffin sulfonates, olefin sulfonates, amine oxides, alpha-sulfonates of fatty acids and of fatty acid esters, alkyl glycosides, ethoxylated alcohols and ethoxylated alkyl phenols, and the like, which are well-known from the detergency art. In general, such detersive surfactants contain an alkyl group in the C.sub.9 -C.sub.18 range; the anionic detersive surfactants can be used in the form of their sodium, potassium or triethanolammonium salts. Standard texts such as the McCutcheon's Index contain detailed listings of such typical detersive surfactants. C.sub.11 -C.sub.14 alkyl benzene sulfonates, C.sub.12 -C.sub.18 paraffinsulfonates, and C.sub.11 -C.sub.18 alkyl sulfates and alkyl ether sulfates are especially preferred in the compositions of the present type.

Also useful herein are the water-soluble soaps, e.g., the common sodium and potassium coconut or tallow soaps well-known in the art. Unsaturated soaps such as alkyl soaps may be used, especially in liquid formulations. Saturated or unsaturated C.sub.9 -C.sub.16 hydrocarbyl succinates are also effective.

The surfactant component can comprise as little as about 1% to as much as about 98% of the detergent compositions herein, depending upon the particular surfactant(s) used and the effects desired. Generally the compositions will contain about 5% to about 60%, more preferably about 6% to 30%, of surfactant. Mixtures of the anionics, such as the alkylbenzene sulfonates, alkyl sulfates and paraffin sulfonates, with C.sub.9 -C.sub.16 ethoxylated alcohol surfactants are preferred for through-the-wash cleansing of a broad spectrum of soils and stains from fabric.

Combinations of anionic, cationic and nonionic surfactants can generally be used. Such combinations, or combinations only of anionic and nonionic surfactants, are preferred for liquid detergent compositions. Such surfactants are often used in acid form and neutralized during preparation of the liquid detergent composition. Preferred anionic surfactants for liquid detergent compositions include linear alkyl benzene sulfonates, alkyl sulfates, and alkyl ethoxylated sulfates. Preferred nonionic surfactants include alkyl polyethoxylated alcohols.

Anionic surfactants are preferred for use as detergent surfactants in granular detergent compositions. Preferred anionic surfactants include linear alkyl benzene sulfonates and alkyl sulfates. Combinations of anionic and nonionic detersive surfactants are especially useful for granular detergent applications.

Detersive Adjuncts: The compositions herein can contain other ingredients which aid in their cleaning performance. For example, it is highly preferred that the laundry compositions herein also contain enzymes to enhance their through-the-wash cleaning performance on a variety of soils and stains. Amylase and protease enzymes suitable for use in detergents are well-known in the art and in commercially available liquid and granular detergents. Commercial detersive enzymes (preferably a mixture of amylase and protease) are typically used at levels of 0.001% to 2%, and higher, in the present compositions.

Moreover, the compositions herein can contain, in addition to ingredients already mentioned, various other optional ingredients typically used in commercial products to provide aesthetic or additional product performance benefits. Typical ingredients include pH regulants, perfumes, dyes, bleaches, optical brighteners, polyester soil release agents, fabric softeners, hydrotropes and gel-control agents, freeze-thaw stabilizers, bactericides, preservatives, suds control agents, bleach activators and the like.

Other Detersive Adjuncts: Optionally, the fully-formulated detergent compositions herein can contain various metal ion sequestering agents such as amine chelants and phosphonate chelants, such as diethylenetriamine pentaacetates, the alkylene amino phosphonates such as ethylenediamine tetraphosphonate, and the like. Clay softeners such as the art-disclosed smectite clays, and combinations thereof with amines and quaternary ammonium compounds can be used to provide softening-through-the-wash benefits. Adjunct builders can be used at typical levels of 5-50%. Such materials include 1-10 micron Zeolite A; 2,2'-oxodisuccinate, tartrate mono- and di-succinates, citrates, C.sub.8 --C.sub.14 hydrocarbyl succinates, sodium tripolyphosphate, pyrophosphate, carbonate, and the like. Inorganic salts such as magnesium sulfate can also be present.

In a through-the-wash fabric laundry mode, the laundry detergent compositions are typically used at a concentration of about 0.10% to about 2.5%, in an aqueous laundry bath, typically at pH 7-11, to launder fabrics. The laundering can be carried out by agitating fabrics with the present compositions over the range from 50.degree. C. to the boil, with excellent results, especially at temperatures in the range from about 35.degree. C. to about 80.degree. C.

The following abbreviations are used in the Examples hereafter:

Highly desirable optional ingredients also include proteolytic enzyme (alcalase, Maxatase, Savinase, Amylase {Termamyl}) and brighteners (DMS/CBS, e.g., disodium 4,4'-bis(2-morpholino-4-anilino-5-triazin-6-ylamino)-stilbene-2:2'-disulfo nate). The balance of the compositions comprises water and minor ingredients such as perfumes; silicone/silica or soap, e.g., tallow fatty acid suds suppressors; Polyoxyethylene Glycols, e.g., PEG-8000; and hydrotropes, e.g., sodium toluene sulfonate.

For each of A-L, an aqueous mixture is prepared by coadding the ingredients, at the indicated weight percentages above, the product of Example 17 in each instance being added last. City water is used to prepare the solutions.

Laundry baths are then prepared having 1,500 ppm of each solution by further diluting the mixtures in the same city water (hardness 12 grains/gallon). Fabrics are added thereto and are laundered at 125.degree. F. (52.degree. C.) in a Terg-O-Tometer (U.S. Testing Co.).

The product of Examples 6-16 and 18 are each substituted for the product of Example 17.

A liquid detergent composition for household laundry use is as follows:

The components are added together with continuous mixing to form the composition.

The product of Example 18 is substituted for the product of Example 17 with equivalent results.

A liquid detergent composition for household laundry use is prepared by mixing the following ingredients:

Granular detergent compositions of Examples 22-39 are prepared as follows. A base powder composition is first prepared by mixing all components except, where present, Dobanol 45E7, bleach, bleach activator, enzyme, suds suppressor, phosphate and carbonate in crutcher as an aqueous slurry at a temperature of about 55.degree. C. and containing about 35% water. The slurry is then spray dried at a gas inlet temperature of about 330.degree. C. to form base powder granules. The bleach activator, where present, is then admixed with TAE.sub.25 as binder and extruded in the form of elongated "noodles" through a radial extruder as described in U.S. Pat. No. 4,399,049, Gray et al, issued Aug. 16, 1983, incorporated herein by reference. The bleach activator noodles, bleach, enzyme, suds suppressor, phosphate and carbonate are then dry-mixed with the base powder composition. Dobanol 45E7 is sprayed into the resulting mixture. Finally, the compound(s) of the present invention are dry-added in freeze-dried form.

This example illustrates a composition of matter comprising a high proportion of especially useful compounds according to the invention, which can be used as dispersants in laundry detergent compositions without further purification. The preferred polyhydric alcohols herein are glucosides. The composition is prepared from starch, ethylene glycol, maleic anhydride and D,L-aspartic acid.

Ethylene glycol and starch are first reacted in the presence of sulfuric acid to prepare mono- and bisethylene glycol glucosides, by an art-known procedure. See F. H Otey, F. L Bennett, B. L Zagoren and C. L Mehltretter, Ind. Eng. Chem. Prod. Res. Develop., Vol. 4, page 224, 1965, incorporated herein by reference. The mono- / bis- ethylene glycol glucoside mixture is now reacted with maleic anhydride, following general procedure 1A, using 3.3 moles of maleic anhydride per mole of starch (anhydroglucose) units of the glucoside mixture, producing a butenedioate half-ester of the glucoside mixture, which is characterized using general procedures 1D and 1E. On the basis of these procedures, Q.sub.1 =7.41.times.10.sup.-3 moles of butenedioate half-ester per gram of sample, and Q.sub.2 =6.59.times.10.sup.-3 moles of acid per gram of sample.

The butenedioate half-ester of the glucoside mixture is reacted with aspartic acid, using the general procedure 2A, to form the product composition.

The structure .of each of the compounds of the invention, actually accounting for the predominant molecules in the chemically stable product composition, is similar to the rather simpler methyl glucoside shown in (X) hereinabove: points of specific difference are that MA- substitution (in this case M=Na and A=--OC(O)C(L)HCH.sub.2 (O)C-- where L is L.sup.1, i.e., aspartate) is not typically absolutely complete; methyl is, of course absent since the moiety E here is one based on an oxyethyleneoxy-starch unit (in the glycol-alpha-D-glucoside and glycol-beta-D-glucoside forms of the novel compounds); or on a starch-oxyethyleneoxy-starch unit (in the glycol diglucoside form, which is especially preferred). The quantity n as given in the general formula of the compounds of the invention is, in this specific example, in the range 5-8.

The better to visualise the composition, the artisan is referred to the stuctural diagram given by Otey et al, I&EC Product Research and Development, 1965, Vol. 4, at page 228, incorporated by reference. Albeit rather complex, this structure diagram represents the known starting glucoside mixture derived from starch and ethylene glycol as it exists prior to functionalization with maleic anhydride and aspartate in the manner of the instant invention. What is effectively achieved in the instant Example is to produce an excellent and inexpensive dispersant for laundry products by replacing a major proportion of the --OH moieties shown in the Otey et al structure with --OA.crclbar.M.sym. moieties as defined supra.