Phenyl Sulfonate Esters as Peroxygen Activators

This invention relates to active oxygen compositions. In particular, the invention is concerned with activated peroxygen compounds and their application to laundering operations.

The use of bleaching agents as laundering aids is well known. In fact, such entities are considered necessary adjuncts for cleaning today's fabrics which embrace a wide spectrum of synthetic, natural and modified natural fiber systems, each differing in washing characteristics.

Laundry bleaches generally fall into one of two categories; active oxygen-releasing or peroxygen and active chlorine-releasing. Of the two, the chlorine bleach is more likely to react with the various components of a detergent washing formulation than peroxygen bleaches. Moreover, fabrics treated with chlorine bleaches exhibit significant loss of strength and depending on the frequency of bleaching, the useful life of the cloth may be appreciably reduced; with dyed fabrics, colors are often degraded. Another objection to chlorine bleaches is their pronounced tendency to cause yellowing, particularly with synthetics and resin treated fabrics. Peroxygen bleaches are substantially free of such adverse side effects.

Despite their many advantages, bleaching agents of the active oxygen-releasing type are as a class not optimally effective until use temperatures exceed about 85.degree. C., usually 90.degree. C., or higher. This rather critical temperature-dependency of peroxygen bleaching agents and especially the persalt bleaches such as sodium perborate poses a rather serious drawback since many household washing machines are now being operated at water temperatures less than about 60.degree. C., well below those necessary to render bleaching agents such as the perborates adequately effective. Although the near boiling washing temperatures employed in Europe and some other countries favor the use of peroxygen bleaches, it can be expected that such temperatures will be lowered in the interest of conserving energy. Consequently, where a comparatively high order of bleaching activity at reduced temperature is desired, resort must be had to chlorine bleaches despite their attendant disadvantages, i.e., impairment of fabric strength, fabric discoloration, etc.

In an effort to realize the full potential of peroxygen bleaches, such materials have been the focus of considerable research and development effort over the years. One result of these investigations was the finding that certain substances, activators as they are usually called, have the capacity of amplifying the bleaching power of peroxygen compounds below about 60.degree. C. where many home washing machines are commonly operated, or preferably operated. Although the precise mechanism of peroxygen bleach activation is not known, it is believed that activator-peroxygen interaction leads to the formation of an intermediate species which constitutes the active bleaching entity. In a sense, then, the activator-peroxygen component functions as a precursor system by which the in situ generation of species providing effective bleaching means is made possible.

Although numerous compounds have been proposed and tested as peroxygen bleach activators, a satisfactory candidate has thus far not been forthcoming. Perhaps the primary objection is the failure to provide the desired degree of bleaching activity within the limitations imposed by economically feasible practice. Thus, it is often necessary to utilize the activator compound in inordinately high concentrations in order to achieve satisfactory results; in other instances, it is found that a given activator is not generally applicable and thus may be used advantageously only in conjunction with rather specific and delimited types of peroxygen bleaching agents. Other disadvantages characterizing many of the activator compounds thus far contemplated include, for example, the difficulties associated with their incorporation into detergent powder compositions including stability problems and short shelf life. Since many of the activators are liquids under normal conditions, the blending of such materials into solid products is not practical, at least so far as home application is concerned. Moreover, ancillary techniques specifically devised for purposes of facilitating activator-detergent powder blending in such instances are often economically prohibitive, the results obtained failing to justify the involved costs.

Classes of compounds which are representative of prior art activators for peroxygen bleaches include carboxylic acid anhydrides disclosed in U.S. Pat. Nos. 2,284,477, 3,532,634 and 3,298,775; carboxylic esters disclosed in U.S. Patent No. 2,955,905; N-substituted, N-acylnitrobenzenesulfonamides disclosed in U.S. Pat. No. 3,321,497; N-benzoyIsaccharin disclosed in U.S. Pat. No. 3,886,078; N-acyl compounds such as those described in U.S. Pat. No. 3,912,648 and 3,919,102 and aromatic sulfonyl chlorides disclosed in Japanese Pat. Publication No. 90980 of Nov. 27, 1973.

While certain of these activators are effective in varying degrees, there is a continuing need for candidate compounds of improved performance and properties.

It has now been discovered that the bleaching capacity of peroxygen bleaches at low temperatures is increased by contacting them with a phenyl sulfonate ester activator compound and the provisions of bleaching compositions containing such components and the use thereof alone or in conjunction with conventional laundering processes and materials to treat soiled and/or stained fabrics constitutes the principal object and purpose of the invention. Other objects and purposes will become apparent subsequently herein.

The phenyl sulfonate ester activator compounds aforesaid can be depicted by the following formula: ##STR2## wherein R is selected from the class consisting of a hydrocarbon radical of 1 to 16 carbon atoms and a heterocyclic radical having 1 ring or 2 fused rings, said ring or rings containing 5 to 6 members of which 1 to 2 are heteroatoms selected from the group consisting of nitrogen, oxygen and sulfur; X is hydrogen or at least one electron withdrawing substituent and n is an integer of from 1 to 5.

Although the herein phenyl sulfonate esters bearing no substituents exhibit some degree of peroxygen activation, those members of the formula wherein X represents at least one electron-withdrawing group are the most effective. Exemplary electron-withdrawing groups include nitro, sulfonyloxy, acyl, chloro, bromo, cyano and carbonylmethoxy.

Another proviso attached to the characterization of the herein activators is that they exhibit sufficient solubility in the bleaching system in order to provide the requisite degree of activation for the active oxygen-releasing bleaching agent. For instance, introducing bulky substituents into R and the phenyl ring of the formula may give rise to a derivative of low solubility. In general, compounds containing two aromatic rings tend to be sparingly soluble under bleaching conditions. Also, the particular type of substituent may also be a factor affecting the solubility factor.

The peroxygen bleach activators of the invention are prepared by combining the appropriate phenol with an alkyl- or arylsulfonyl chloride in the presence of a tertiary amine acid acceptor in dichloromethane solvent at 0.degree. C., as described by J. C. Carnahan and coworkers (J. Am. Chem. Soc., 98, 2526, 1976). The general reaction can be depicted in accordance with the following scheme: ##STR3##

After the reaction is complete, the solvent is removed, the mixture poured into ice water and the resulting crude material separated, dried and purified by crystallization from a liquid organic solvent such as a lower alcohol, e.g. ethanol, an aromatic or aliphatic hydrocarbon, such as benzene or heptane or mixtures thereof, a chlorinated hydrocarbon or the like. The purified products tend to be crystalline solids which can be identified by melting point and chemical and instrumental analysis, e.g. IR and NMR spectroscopy.

R in the formula is desirably alkyl of 1 to 16 carbon atoms, phenyl, naphthyl or a heterocyclic ring as above defined. R can also be cycloalkyl of 3 to 7 carbon atoms such as cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl. Although R can be unsaturated, it should not contain carbon-carbon multiple bonds of the type which polymerize under conditions of bleaching. R can also contain solubilizing substituents of the type specified for the phenyl group of the formula.

A class of phenyl sulfonate esters herein which have been found particularly effective as peroxygen activators are the phenyl esters of alkanesulfonic acids of 1 to 16 carbon atoms and benzenesulfonic acid bearing the aforeenumerated solubilizing groups.

Illustrative examples of some specific phenyl sulfonate esters falling within the ambit of the formula aforesaid and which are useful as peroxygen activators in practicing the invention are:

1,2-dibromoethanesulfonic acid p-chlorophenyl ester

Ethanesulfonic acid 2-chloro-6-nitrophenyl ester

1,2,2-tribromoethanesulfonic acid p-chlorophenyl ester

Methanesulfonic acid o-bromophenyl ester

Methanesulfonic acid p-bromophenyl ester

Methanesulfonic acid 2-bromo-6-nitrophenyl ester

p-methoxycarbonylbenzenesulfonic acid 2-bromo-6-nitrophenyl ester

Decanesulfonic acid p-nitrophenyl ester

1-octanesulfonic acid 2,4-dichlorophenyl ester

1-butanesulfonic acid o-chlorophenyl ester

1-butanesulfonic acid 2-chloro-6-nitrophenyl ester

p-hydroxybenzenesulfonic acid o-nitrophenyl ester

p-acetylbenzenesulfonic acid o-chlorophenyl ester

p-decylbenzenesulfonic acid p-chlorophenyl ester

2,4-dichlorobenzenesulfonic acid p-hydroxyphenyl ester

p-ethoxybenzenesulfonic acid p-cyanophenyl ester

p-hydroxybenzenesulfonic acid 4-bromo-2-chlorophenyl ester

p-chlorobenzenesulfonic acid 3-bromo-4-chlorophenyl ester

p-methoxycarbonylbenzenesulfonic acid 3-bromo-2,4-dichlorophenyl ester

Methanesulfonic acid 2-bromo-4-fluorophenyl ester

1-butanesulfonic acid 2-sec-butyl-4,6-dinitrophenyl ester

p-chlorobenzenesulfonic acid 4-chloro-2-ethoxyphenyl ester

2-octanesulfonic acid p-methoxycarbonylphenyl ester

1-hexanesulfonic acid p-sulfonyloxyphenyl ester

p-chlorobenzenesulfonic acid p-acetylphenyl ester

2-thiophenesulfonic acid p-hydroxphenyl ester

2-acetylhexadecylsulfonic acid p-nitrophenyl ester

Benzenesulfonic acid p-sulfophenyl ester

2-quinolinesulfonic acid p-hydroxylphenyl ester

Cyclohexanesulfonic acid 2,4-dichloro-5-hydroxyphenyl ester

Benzene disulfonic acid mono-p-chlorophenyl ester

In accordance with the invention, low temperature bleaching (i.e. below about 60.degree. C.) of stained and/or soiled fabrics is effected by contacting them with a solution containing a phenyl sulfonate ester activator herein and an active oxygen-releasing compound. The active oxygen-releasing compounds include such peroxygen compounds as hydrogen peroxide or those peroxygen compounds that liberate hydrogen peroxide in aqueous media. Examples of such peroxygen compounds are urea peroxide, alkali metal perborates, percarbonates, perphosphates, persulfates, monopersulfates and the like. Combinations of two or more peroxygen bleaches can be used where desired. The same holds true in the case of the activators. Although any number of peroxygen compounds are suitable in carrying out the invention, a preferred compound is sodium perborate tetrahydrate, since it is a readily available commercial product. Another suitable persalt is sodium carbonate peroxide.

Sufficient peroxygen compounds to provide from about 2 ppm to 2,000 ppm active oxygen in solution are used. For home bleaching applications, the concentration of active oxygen in the wash water is desirably from about 5 to 100 ppm, preferably about 15 to 60 ppm. Sodium perborate tetrahydrate, the preferred peroxygen compound, contains 10.4% active oxygen. The actual concentration employed in a given bleaching solution can be varied widely, depending on the intended use of the solution.

The concentration of the phenyl sulfonate esters in the bleaching solution depends to a large extent on the concentration of the peroxygen compound which, in turn, depends on the particular use for which a given composition is formulated. Higher or lower levels can be selected according to the needs of the formulator. Overall, increased bleaching results are realized when the active oxygen of the peroxygen compound and phenyl sulfonate ester are present in a mole ratio in the range of from about 20:1 to 1:3, preferably from about 10:1 to 1:1.

Activation of the peroxygen bleaches is generally carried out in aqueous solution at a pH of from about 6 to about 12, most preferably 8.0 to 10.5. Since an aqueous solution of persalts or peracids is generally acidic, it is necessary to maintain the requisite pH conditions by means of buffering agents. Buffering agents suitable for use herein include any non-interfering compound which can alter and/or maintain the solution pH within the desired range, and the selection of such buffers can be made by referring to a standard text.

For instance, phosphates, carbonates, or bicarbonates, which buffer within the pH range of 6 to 12 are useful. Examples of suitable buffering agents include sodium bicarbonate, sodium carbonate, sodium silicate, disodium hydrogen phosphate, sodium dihydrogen phosphate. The bleach solution may also contain a detergent agent where bleaching and laundering of the fabric is carried out simultaneously. The strength of the detergent agent is commonly about 0.05% to 0.80% (wt.) in the wash water.

Although the activator, buffer and peroxygen compound can be employed individually in formulating the bleach solutions of the invention, it is generally more convenient to prepare a dry blend of these components and the resulting composition added to water to produce the bleach solution. A soap or organic detergent can be incorporated into the composition to give a solution having both washing and bleaching properties. Organic detergents suitable for use in accordance with the present invention encompass a relatively wide range of materials and may be of the anionic, non-ionic, cationic or amphoteric types.

The anionic surface active agents include those surface active or detergent compounds which contain an organic hydrophobic group and an anionic solubilizing group. Typical examples of anionic solubilizing groups are sulfonate, sulfate, carboxylate, phosphonate and phosphate. Examples of suitable anionic detergents which fall within the scope of the invention include the soaps, such as the water-soluble salts of higher fatty acids or rosin acids, such as may be derived from fats, oils, and waxes of animal, vegetable or marine origin, e.g., the sodium soaps of tallow, grease, coconut oil, tall oil and mixtures thereof; and the sulfated and sulfonated synthetic detergents, particularly those having about 8 to 26, and preferably about 12 to 22, carbon atoms to the molecule.

As examples of suitable synthetic anionic detergents the higher alkyl mononuclear aromatic sulfonates are preferred particularly the LAS type such as the higher alkyl benzene sulfonates containing from 10 to 16 carbon atoms in the alkyl group, e.g., the sodium salts such as decyl, undecyl, dodecyl (lauryl), tridecyl, tetradecyl, pentadecyl, or hexadecyl benzene sulfonate and the higher alkyl toluene, xylene and phenol sulfonates; alkyl naphthalene sulfonate, ammonium diamyl naphthalene sulfonate, and sodium dinonyl naphthalene sulfonate.

Other anionic detergents are the olefin sulfonates including long chain alkene sulfonates, long chain hydroxyalkane sulfonates or mixtures of alkenesulfonates and hydroxyalkanesulfonates. These olefin sulfonate detergents may be prepared, in known manner, by the reaction of SO.sub.3 with long chain olefins (of 8-25 preferably 12-21 carbon atoms) of the formula RCH-CHR.sub.1, where R is alkyl and R.sub.1 is alkyl or hydrogen, to produce a mixture of sultones and alkenesulfonic acids, which mixture is then treated to convert the sultones to sulfonates. Examples of other sulfate or sulfonate detergents are paraffin sulfonates, such as the reaction products of alpha olefins and bisulfites (e.g. sodium bisulfite), e.g., primary paraffin sulfonates of about 10-20 preferably about 15-20 carbon atoms; sulfates of higher alcohols; salts of .alpha.-sulfofatty esters (e.g., of about 10 to 20 carbon atoms, such as methyl .alpha.-sulfomyristate or .alpha.-sulfotallowate).

Examples of sulfates of higher alcohols are sodium lauryl sulfate, sodium tallow alcohol sulfate; Turkey Red Oil or other sulfated oils, or sulfates of mono- or diglycerides of fatty acids (e.g. stearic monoglyceride monosulfate), alkyl poly(ethenoxy) ether sulfates such as the sulfates of the condensation products of ethylene oxide and lauryl alcohol (usually having 1 to 5 ethenoxy groups per molecule); lauryl or other higher alkyl glyceryl ether sulfonates; aromatic poly(ethenoxy) ether sulfates such as the sulfates of the condensation products of ethylene oxide and nonyl phenol (usually having 1 to 20 oxyethylene groups per molecule, preferably 2-12).

The suitable anionic detergents include also the acyl sarcosinates (e.g. sodium lauroylsarcosinate) the acyl ester (e.g. oleic acid ester) of isethionates, and the acyl N-methyl taurides (e.g. potassium N-methyl lauroyl or oleyl tauride).

Other highly preferred water soluble anionic detergent compounds are the ammonium and substituted ammonium (such as mono-, di- and triethanolamine), alkali metal (such as sodium and potassium) and alkaline earth metal (such as calcium and magnesium) salts of the higher alkyl sulfates, and the higher fatty acid monoglyceride sulfates. The particular salt will be suitably selected depending upon the particular formulation and the proportions therein.

Nonionic surface active agents include those surface active or detergent compounds which contain an organic hydrophobic group and a hydrophilic group which is a reaction product of a solubilizing group such as carboxylate, hydroxyl, amido or amino with ethylene oxide or with the polyhydration product thereof, polyethylene glycol.

As examples of nonionic surface active agents which may be used there may be noted the condensation products of alkyl phenols with ethylene oxide, e.g., the reaction product of octyl phenol with about 6 to 30 ethylene oxide units; condensation products of alkyl thiophenols with 10 to 15 ethylene oxide units; condensation products of higher fatty alcohols such as tridecyl alcohol with ethylene oxide; ethylene oxide addends of monoesters of hexahydric alcohols and inner ethers thereof such as sorbitol monolaurate, sorbitol mono-oleate and mannitol monopalmitate, and the condensation products of polypropylene glycol with ethylene oxide.

Cationic surface active agents may also be employed. Such agents are those surface active detergent compounds which contain an organic hydrophobic group and a cationic solubilizing group. Typical cationic solubilizing groups are amine and quaternary groups.

As examples of suitable synthetic cationic detergents there may be noted the diamines such as those of the type RNHC.sub.2 H.sub.4 NH.sub.2 wherein R is an alkyl group of about 12 to 22 carbon atoms, such as N-2-aminoethyl stearyl amine and N-2-aminoethyl myristyl amine; amide-linked amines such as those of the type R.sub.1 CONHC.sub.2 H.sub.4 NH.sub.2 wherein R is an alkyl group of about 9 to 20 carbon atoms, such as N-2-amino ethyl stearyl amide and N-amino ethyl myristyl amide; quaternary ammonium compounds wherein typically one of the groups linked to the nitrogen atom are alkyl groups which contain 1 to 3 carbon atoms, including such 1 to 3 carbon alkyl groups bearing inert substituents, such as phenyl groups, and there is present an anion such as halide, acetate, methosulfate, etc. Typical quaternary ammonium detergents are ethyl-dimethyl-stearyl ammonium chloride, benzyl-dimethyl-stearyl ammonium chloride, benzyl-diethyl-stearyl ammonium chloride, trimethyl stearyl ammonium chloride, trimethyl-cetyl ammonium bromide, dimethylethyl dilauryl ammonium chloride, dimethyl-propyl-myristyl ammonium chloride, and the corresponding methosulfates and acetates.

Examples of suitable amphoteric detergents are those containing both an anionic and a cationic group and a hydrophobic organic group, which is advantageously a higher aliphatic radical, e.g., of 10-20 carbon atoms. Among these are the N-long chain alkyl aminocarboxylic acids e.g. of the formula ##STR4## the N-long chain alkyl iminodicarboxylic acids (e.g. of the formula RN(R'COOH).sub.2) and the N-long chain alkyl betaines e.g. of the formula ##STR5## where R is a long chain alkyl group, e.g. of about 10-20 carbons, R' is a divalent radical joining the amino and carboxyl portions of an amino acid (e.g. an alkylene radical of 1-4 carbon atoms), H is hydrogen or a salt-forming metal, R.sub.2 is a hydrogen or another monovalent substitutent (e.g. methyl or other lower alkyl), and R.sub.3 and R.sub.4 are monovalent substituents joined to the nitrogen by carbon-to-nitrogen bonds (e.g. methyl or other lower alkyl substituents). Examples of specific amphoteric detergents are N-alkyl-beta-aminopropionic acid; N-alkyl-beta-iminodipropionic acid, and N-alkyl, N,N-dimethyl glycine; the alkyl group may be, for example, that derived from coco fatty alcohol, lauryl alcohol, myristyl alcohol (or a lauryl-myristyl mixture), hydrogenated tallow alcohol, cetyl, stearyl, or blends of such alcohols. The substituted aminopropionic and iminodipropionic acids are often supplied in the sodium or other salt forms, which may likewise be used in the practice of this invention. Examples of other amphoteric detergents are the fatty imidazolines such as those made by reacting a long chain fatty acid (e.g. of 10 to 20 carbon atoms) with diethylene triamine and monohalocarboxylic acids having 2 to 6 carbon atoms, e.g. 1-coco-5-hydroxyethyl-5-carboxymethylimidazoline; betaines containing a sulfonic group instead of the carboxylic group; betaines in which the long chain substituent is joined to the carboxylic group without an intervening nitrogen atom, e.g. inner salts of 2-trimethylamino fatty acids such as 2-trimethylaminolauric acid, and compounds of any of the previously mentioned types but in which the nitrogen atom is replaced by phosphorus.

The instant compositions optionally contain a detergency builder of the type commonly added to detergent formulations. Useful builders herein include any of the conventional inorganic and organic water-soluble builder salts. Inorganic detergency builders useful herein include, for example, water-soluble salts of phosphates, pyrophosphates, orthophosphates, polyphosphates, silicates, carbonates, zeolites, including natural and synthetic and the like. Organic builders include various water-soluble phosphonates, polyphosphonates, polyhydroxysulfonates, polyacetates, carboxylates, polycarboxylates, succinates, and the like.

Specific examples of inorganic phosphate builders include sodium and potassium tripolyphosphates, phosphates, and hexametaphosphates. The organic polyphosphonates specifically include, for example, the sodium and potassium salts of ethane 1-hydroxy-1,1-diphosphonic acid and the sodium and potassium salts of ethane-1,1,2-triphosphonic acid. Examples of these and other phosphorus builder compounds are disclosed in U.S. Pat. Nos. 3,159,581, 3,213,030, 3,422,021, 3,422,137, 3,400,176 and 3,400,148, incorporated herein by reference. Sodium tripolyphosphate is an especially preferred, water-soluble inorganic builder herein.

Non-phosphorus containing sequestrants can also be selected for use herein as detergency builders.

Specific examples of non-phosphorus, inorganic builder ingredients include water-soluble inorganic carbonate, bicarbonate, and silicate salts. The alkali metal, e.g. sodium and potassium, carbonates, bicarbonates, and silicates are particularly useful herein.

Water-soluble, organic builders are also useful herein. For example, the alkali metal, ammonium and substituted ammonium polyacetates, carboxylates, polycarboxylates and polyhydroxysulfonates are useful builders in the present compositions and processes. Specific examples of the polyacetate and polycarboxylate builder salts include sodium, potassium, lithium, ammonium and substituted ammonium salts of ethylenediaminetetraacetic acid, nitrilotriacetic acid, oxydisuccinic acid, mellitic acid, benzene polycarboxylic (i.e., penta- and tetra-) acids, carboxymethoxysuccinic acid and citric acid.

Highly preferred non-phosphorus builder materials (both organic and inorganic) herein include sodium carbonate, sodium bicarbonate, sodium silicate, sodium citrate, sodium oxydisuccinate, sodium mellitate, sodium nitrilotriacetate, and sodium ethylenediaminetetraacetate, and mixtures thereof.

Other preferred organic builders herein are the polycarboxylate builders set forth in U.S. Pat. No. 3,308,067, incorporated herein by reference. Examples of such materials include the water-soluble salts of homo- and copolymers of aliphatic carboxylic acids such as maleic acid, itaconic acid, mesaconic acid, fumaric acid, aconitic acid, citraconic acid and methylenemalonic acid.

The builders aforesaid, particularly the inorganic types, can function as buffers to provide the requisite alkalinity for the bleaching solution. Where the builder does not exhibit such buffer activity, an alkaline reacting salt can be incorporated in the formulation.

The dry blend compositions of the invention contain about 0.1 to 50% (wt.), preferably 0.5 to 20% (wt.) of the herein phenyl sulfonate ester activator. It will be appreciated that the concentration of activator will depend on the concentration of the peroxygen bleach compound which is governed by the particular degree of bleaching desired. Higher or lower levels within the range will be selected to meet the requirement of the formulator. As to the peroxygen bleaching agent, this is present to the extent of about 1 to 75% (wt.) of the composition, depending on the degree of bleaching activity desired. Generally speaking, optimal bleaching is obtained when the compositions are formulated with a peroxygen/phenyl sulfonate ester mole ratio in the range of from about 20:1 to 1:3, preferably about 10:1 to about 1:1. The composition will contain a buffering agent in sufficient quantity to maintain a pH of about 6 to 12 when the composition is dissolved in water. The buffering agent can constitute from about 1% to about 95% (wt.) of the dry blended composition.

The herein activated bleach compositions can be provided for use in combination with a detergent agent or as a fully-formulated built detergent. Such compositions will comprise from about 5 to 50% of the activated bleach system, from about 5 to 50% (wt.) of the detergent agent and optionally from about 1 to 60% (wt.) of a detergency builder which can also function as a buffer to provide the requisite pH range when the composition is added to water.

The compositions herein can include detergent adjunct materials and carriers commonly found in laundering and cleaning compositions. For example, various perfumes, optical brighteners, fillers, anti-caking agents, fabric softeners, and the like can be present to provide the usual benefits occasioned by the use of such materials in detergent compositions. Enzymes, especially the thermally stable proteolytic and lipolytic enzymes used in laundry detergents, also can be dry-mixed in the compositions herein.

The solid peroxygen bleaching compositions herein are prepared by simply admixing the ingredients. When preparing mixed detergent/bleaches, the peroxygen and activator can be mixed either directly with the detergent compound, builder, etc., or the peroxygen and activator can be separately or collectively coated with a water-soluble coating material to prevent premature activation of the bleaching agent. The coating process is conducted according to known procedures in the art utilizing known coating materials. Suitable coating materials include compounds such as magnesium sulfate hydrate, polyvinyl alcohol, or the like.

The following examples are illustrative of the compounds of the invention:

To a chilled solution of 13.6 g (0.1 mole) of p-hydroxyacetophenone in 50 ml of dichloromethane was added 10.1 g (0.1 mole) of triethylamine. A solution of 11.5 g (0.1 mole) of methanesulfonyl chloride in 50 ml of dichloromethane was added dropwise. The mixture was stirred overnight. An additional 2.0 g of methanesulfonyl chloride was added and the mixture was heated to 40.degree. C. Dichloromethane was removed in a rotary evaporator. The residue was stirred in ice water. The precipitated product was removed by filtration and dried, giving 18.5 g (86% yield) of crude ester. The crude product was dissolved in 30 ml of benzene and filtered to remove insoluble impurities. The ester was precipitated by adding 30 ml of cyclohexane; this gave 7.0 g of pure product with m.p. 72.0.degree.-72.3.degree. C. The proton NMR spectrum of the product was in agreement with the proposed structure.

Anal: Calc'd for C.sub.9 H.sub.10 O.sub.4 S: C, 50.47; H, 4.71; S, 14.94. Found: C, 50.21; H, 4.82; S, 14.87.

Using the procedure of Example 1, equimolar quantities (0.1 mole) of 4-acetoxyphenol, triethylamine and benzenesulfonyl chloride were combined in 250 ml of dichloromethane and allowed to react for 2.5 hours. The yield of crude product was 26.0 g (89% yield) of ester with m.p. 59.0.degree.-66.6.degree. C. Crystallization from ethanol:pentane gave 23.0 g of material with m.p. 59.0.degree.-67.4.degree. C. The NMR spectrum was in agreement with the proposed structure.

Anal: Calc'd for C.sub.14 H.sub.12 O.sub.5 S: C, 57.53; H, 4.14; S, 10.97. Found: C, 57.29; H, 4.08; S, 10.94.

Following the procedure of Example 1, equimolar quantities (0.666 mole) of 4-acetoxyphenol, triethylamine and methanesulfonyl chloride were reacted in 130 ml of dichloromethane. The crude product amounted to 12.2 g (81% yield).

A 5 g sample of crude product was crystallized from hot ethanol; yield 4.0 g of pure product with m.p. 93.degree.-95.degree. C. The proton NMR spectrum of the product was in agreement with the structure.

Anal: Calc'd for C.sub.9 H.sub.10 O.sub.5 S: C, 46.96; H, 4.38; S, 13.93. Found: C, 46.88; H, 4.38; S, 14.03.

In a procedure patterned after that of Example 1, equimolar quantities (0.1 mole) of 2-acetoxyphenol, triethylamine and methanesulfonyl chloride were reacted in 100 ml of dichloromethane. The yield of product was 19.6 g (82% yield). The NMR spectrum was consistent with the above depicted structure.

Using the procedure of the previous examples, equimolar quantities (0.10 mole) of p-nitrophenol and methanesulfonyl chloride and a slight excess (0.12 mole) of triethylamine were reacted in 100 ml of dichloromethane. the crude product was recovered after about 1 hour reaction time. On recrystallization from ethanol, there was obtained 17.3 g (80% yield) of sulfonate ester with m.p. 89.degree.-91.degree. C. The proton NMR spectrum was consistent with the structure.

Anal: Calc'd for C.sub.7 H.sub.7 NO.sub.5 S: C, 38.71; H, 3.22; N, 6.45; S, 14.74. Found: C, 38.44; H, 3.28; N, 6.34; S, 14.61.

Following the procedure of the previous examples, equimolar quantities (0.1 mole) of phenol, methanesulfonyl chloride and pyridine were combined and allowed to react for 3 hours at 130.degree. C. The crude product was recrystallized from hexane:benzene (1:4 v/v) giving 5.0 g (29% yield) of product with m.p. 59.5.degree.-61.2.degree. C. The proton NMR spectrum was consistent with the structure.

Anal: Calc'd for C.sub.7 H.sub.8 O.sub.3 S: C, 48.83; H, 4.65; S, 18.60. Found: C, 49.03; H, 4.87; S, 18.22.

Phenyl methanesulfonate (8.6 g; 0.05 mole), prepared by the procedure of Example 6, was dissolved in 30 ml of nitromethane and added dropwise to a solution containing 4.0 g (0.05 mole) of sulfur trioxide and 50 ml of nitromethane. The solution was stirred for 15 minutes. Nitromethane was then removed by distillation under reduced pressure. The residual oil was taken up in 50 ml of methanol and the mixture was cooled to approximately 10.degree. C. A solution of 4.1 g (0.05 mole) of sodium acetate in 50 ml of methanol was added dropwise. The solution was stirred for fifteen minutes. The precipitated product was recovered by filtration and dried, giving 7.9 g (57% yield) of ester. The proton NMR spectrum of the product was consistent with the structure.

Anal: Calc'd for C.sub.7 H.sub.7 O.sub.6 S.sub.2 Na: C, 30.66; H, 2.57; S, 23.28. Found: C, 30.83; H, 2.52; S, 23.08.

Using the procedure of the previous examples, equimolar quantities (0.1 mole) of phenol, p-tolenesulfonyl chloride and pyridine were combined and allowed to react for approximately two hours at 135.degree. C. The crude product was recrystallized from cyclohexane giving 17.2 g (69% yield) of product with m.p. 94.degree. C. The proton NMR spectrum was in agreement with the structure.

Anal: Calc'd for C.sub.13 H.sub.12 SO.sub.3 : C, 62.89; H, 4.83; S, 12.89. Found: C, 63.03; H, 5.10; S, 12.62.

Evaluation of Compounds as Bleach Activators

Compounds of the invention were evaluated for bleach activating efficacy by determining the increase in percent tea stain removal (%TSR) achieved by use of both the peroxygen source and activator compared with that obtained by use of the peroxygen source alone. Both tests were performed under otherwise identical low temperature laundering conditions. The increase in %TSR is called .DELTA.%TSR. The evaluation was carried out in the presence of a detergent formulation and sodium perborate tetrahydrate as the source of peroxygen compound.

Tea-stained cotton and 65% dacron/35% cotton swatches (5.times.5 inches) used in these tests were prepared as follows: For each 50 swatches, 2000 ml of tap water was heated to boiling in a four-liter beaker. Reflectance readings were made on each swatch, using a Hunter Model D-40 Reflectometer before staining. Two family size tea bags were added to each beaker and boiling was continued for five minutes. The tea bags were then removed and 50 fabric swatches were added to each beaker. The dacron/cotton and 100% cotton swatches were boiled in the tea solution for seven and five minutes respectively, after which the entire content of each beaker was transferred to a centrifuge and rotated for about 0.5 minutes.

The swatches were then dried for thirty minutes in a standard household laundry drier. One hundred dry swatches were rinsed four times by agitating manually in 2000 ml portions of cold tap water. The swatches were dried in the household drier for approximately 40 minutes; they were allowed to age for at least 3 days before use. Reflectance readings for each swatch were taken prior to bleaching tests, using a Hunter Model D-40 Reflectometer.

Three stained cotton and polyester/cotton swatches were added to each of several stainless steel Terg-O-Tometer vessels containing 1000 ml of 0.15% detergent solution, maintained at a constant temperature of 105.degree. F. The Terg-O-Tometer is a test washing device manufactured by the U.S. Testing Company. The detergent solution was prepared from a detergent formulation having the following composition (by weight):

25.0% -- Sodium tripolyphosphate

7.5% -- Sodium dodecylbenzenesulfonate (anionic surfactant)

4.0% -- Alcohol ether sulfate (obtained from 1 mole of C.sub.16 -C.sub.18 alcohol with 1 mole ethylene oxide (anionic surfactant)

6.5% -- Alcohol (C.sub.16 -C.sub.18) sulfate (anionic surfactant)

1.3% -- Polyethylene glycol of about 6000 molecular wt.

35.4% -- Sodium sulfate

11.0% -- Sodium silicate

8.0% -- Moisture

0.8% -- Optical brightener

0.5% -- Carboxymethylcellulose

Measured quantities of sodium perborate tetrahydrate were added to each vessel to provide the desired quantity of active oxygen (A.O.) followed by an amount of activator compound to give the bleaching A.O. levels. In each test run, the activator was excluded from at least one Terg-O-Tometer vessel. The pH of each solution was adjusted to about 10.0 with 5% sodium hydroxide solution. The Terg-O-Tometer was operated at 100 cycles per minute for 15 or 30 minutes at the desired temperature. The swatches were then removed, rinsed under cold tap water and dried in a household clothing drier. Reflectance readings were taken on each swatch and percent tea stain removal (%TSR) was calculated as follows: ##EQU1## The increase of %TSR, termed .DELTA.%TSR, was calculated by subtracting the average %TSR in runs where the perborate was present alone, from the average %TSR obtained in runs where both the activator and the perborate were present. The test results are given in Table I. As the .DELTA.%TSR values clearly demonstrate, the activator compounds of the invention markedly improve the percentage of stain removal compared to the peroxygen bleach compound alone.

Pursuant to the requirements of the patent statutes, the principle of this invention has been explained and exemplified in a manner so that it can be readily practiced by those skilled in the art, such exemplification including what is considered to represent the best embodiment of the invention. However, it should be clearly understood that, within the scope of the appended claims, the invention may be practiced by those skilled in the art, and having the benefit of this disclosure, otherwise than as specifically described and exemplified herein.