Biocidal 2-Aryl-1,3-Cyclohexanedione Enol Ester Compounds

This invention relates to novel 2-aryl-1,3-cyclohexanedione enol ester compounds and methods of preparing same. This invention is also directed to miticidal, mite ovicidal, post-emergent herbicidal and pre-emergent herbicidal compositions comprising an acceptable carrier and a pesticidally effective amount of a compound of this invention, as well as to a method of controlling mites and plant pests which comprises subjecting the mites, the eggs of mites and the plant pests to a pesticidally effective amount of a compound of this invention.

More particularly, this invention relates to compounds of the formula: ##STR1## wherein: R.sub.1, R.sub.2, R.sub.4 and R.sub.5 are individually hydrogen, methyl, halogen, or nitro with the proviso that when R.sub.1 is hydrogen or nitro, then R.sub.5 cannot be hydrogen or nitro;

R.sub.3 is hydrogen, methyl, or halogen;

R.sub.6 through R.sub.11 inclusive are individually hydrogen, C.sub.1 to C.sub.8 alkyl, CF.sub.3, unsubstituted phenyl, or

R.sub.8 and R.sub.9 together may form an alkylene or alkenylene chain completing a 3 to 7 membered ring structure; and

R is C.sub.1 -C.sub.17 alkyl, C.sub.4 alkenyl, C.sub.3 -C.sub.9 cycloalkyl, C.sub.1 -C.sub.6 alkyl substituted C.sub.3 -C.sub.6 cycloalkyl, unsubstituted or non-ortho C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy, halo, or nitro substituted phenyl; and compounds of the formula: ##STR2## wherein: R.sub.1 is ethyl;

R.sub.2 to R.sub.5 inclusive are individually hydrogen, methyl, CF.sub.3 or halogen

with the proviso that halogen atoms may not occupy adjacent positions on the aromatic ring;

R.sub.6, R.sub.7, R.sub.10 and R.sub.11 are hydrogen;

R.sub.8 and R.sub.9 are individually hydrogen, unbranched C.sub.1 -C.sub.4 alkyl, isopropyl, tertiary butyl, diethyl methyl, cycloalkyl, CF.sub.3

with the proviso that when R.sub.8 or R.sub.9 ethyl, isopropyl, or diethyl methyl, R is an unbranched C.sub.1 -C.sub.15 alkyl; or

R.sub.8 and R.sub.9 together form a cyclopentyl or cyclohexyl ring

with the proviso that when R.sub.8 and R.sub.9 together form a cyclohexyl ring, R is an unbranched C.sub.1 to C.sub.14 alkyl; and

R is

unbranched C.sub.1 to C.sub.17 alkyl, unsubstituted C.sub.3 -C.sub.6 cycloalkyl,

unbranched C.sub.1 to C.sub.6 alkyl C.sub.3 -C.sub.6 cycloalkyl, tertiary butyl,

unsubstituted or non-ortho C.sub.1 to C.sub.4 alkyl, halo, or nitro substituted phenyl, or ortho-substituted C.sub.1 -C.sub.6 alkyl phenyl or ##STR3## wherein: R.sub.12 is C.sub.1 to C.sub.7 alkyl, and

R.sub.13 and R.sub.14 are individually C.sub.1 to C.sub.3 alkyl.

The following miticidally, mite ovicidally and/or herbicidally active compounds are illustrative of compounds within the purview of the above generic formula and which can be conveniently prepared by the process of this invention simply by selecting appropriate reactants for use in the procedures described below:

2-(2'-Chlorophenyl)-3-(7-phenylheptanoyloxy)-5,5-dimethyl-2-cyclohexenone.

2-(2'-Chlorophenyl)-3-(2'6'-dichlorohexanoyloxy)-2-cyclohexenone

2-(2',4'-Dibromophenyl)-3-(hexanoyloxy)-2-cyclohexenone

2-(2'-Chlorophenyl)-3-(2-ethylhexanoyloxy)-2-cyclohexenone

2-(2'-Chlorophenyl)-3-benzoyloxy-5,5-dimethyl-2-cyclohexenone

2-(2'-Bromophenyl)-3-(4'-chlorobenzoyloxy)-5,5-dimethyl-2-cyclohexenone

2-(2'-chlorophenyl)-3-(5'-diethylaminophenylcarbonyloxy)-5,5-dimethyl-2-cyc lohexenone

2-(2'-Chlorophenyl)-3-(4'-chlorophenylcarbonyloxy)-5,5-dimethyl-2-cyclohexe none

2-(2'-chloro-5'-nitrophenyl)-3-(4'-dimethylaminophenylcarbonyloxy)-5,5-dime thyl-2-cyclohexenone

2-(2'-Chlorophenyl)-3-(trifluoroacetoxy)-5,5-dimethyl-2-cyclohexenone

2-(2'-Chlorophenyl)-3-(acetoxy)-5,5-dimethyl-2-cyclohexenone

2-(2',4'-Dimethylphenyl)-3-hexanoyloxy-5,5-dimethyl-2-cyclohexenone

2-(2',4'-Dimethylphenyl)-3-(2-ethylhexanoyloxy)-5,5-dimethyl-2-cyclohexenon e

2-(2',3'-Dimethylphenyl)-3-stearoyloxy-5,5-dimethyl-2-cyclohexenone

2-(2',5'-Dichlorophenyl)-3-acetoxy-5,5-dimethyl-2-cyclohexeneone

2-(2',4'-Dibromophenyl)-3-isobutyryloxy-5,5-dimethyl-2-cyclohexenone

2-(2',6'-Dichlorophenyl)-3-hexanoyloxy-5,5-dimethyl-2-cyclohexenone

2-(2',6'-Dichlorophenyl)-3-(2-ethylhexanoyloxy)-5,6-dimethyl-2-cyclohexenon e

2-(2',5'-Dichlorophenyl)-3-stearoyloxy-5,5-dimethyl-2-cyclohexenone

2-(2',3'-Dimethylphenyl)-3-benzoyloxy-5,5-dimethyl-2-cyclohexenone

2-(2',4'-Dimethylphenyl)-3-phenylcarbonyloxy-4,6-dimethyl-2cyclohexenone

2-(2',4'-Dimethylphenyl)-3-(4'-dimethylaminophenylcarbonyloxy-5,5-dimethyl- 2-cyclohexenone

2-(2',4'-Dimethylphenyl)-3-(4'-chlorophenylcarbonyloxy)-5,6-dimethyl-2-cycl ohexenone

2-(2',4'-Dimethylphenyl)-3-trifluoroacetoxy-5,5-dimethyl-2-cyclohexenone

2-(2',4'-Dimethylphenyl)-3-(2-cyclohexenylcarbonyloxy)-5,5-dimethyl-2-cyclo hexenone

2-(2'-Chlorophenyl)-3-acetoxy-5,5-dimethyl-2-cyclohexenone

2-(2'-Chlorophenyl)-3-(cyclopropylcarbonyloxy)-4,5-dimethyl-2-cyclohexenone

2-(2'-Bromophenyl)-3-(2-ethylhexanoyloxy)-5,6-dimethyl-2-cyclohexenone

2-(2'-Methylphenyl)-3-(4'-methoxyphenylcarbonyloxy)-5,5-dimethyl-2-cyclohex enone

2-(2',4'-Dimethylphenyl)-3-(3'-nitrophenylcarbonyloxy)-5,5-dimethyl-2-cyclo hexenone

2-(2'-Methyl-4'-chlorophenyl)-3-trifluoroacetoxy)-5,5-dimethyl-2-cyclohexen one

2-(2',4',6'-Trimethylphenyl)-3-cyclopropylcarbonyloxy-5,5-dimethyl-2-cycloh exenone

2-(2',4',6'-Trimethylphenyl)-3-(2-cyclohexenylcarbonyloxy)-5,5-dimethyl-2-c yclohexenone

4-Acetoxy-3-(2',4'-dimethylphenyl)-bicyclo[3.2.1]oct-3-en-2one

4-(2-Ethylhexanoyloxy)-3-(2'-chlorophenyl)-spiro[5.5]undec-3-en-2-one

2-Hexanoyloxy-3-(2',4'-dichlorophenyl)-bicyclo[4.4.0]dec-2-en-4one

3-Isobutyryloxy-4-(4'-chlorphenyl)-2-(2',5'-dimethylphenyl)-2-cyclohexenone

All compounds within the purview of the above generic formulae exhibit miticidal, mite ovicidal and herbicidal activity to a lesser or greater extent. Some of these compounds exhibit very powerful miticidal, mite ovicidal or herbicidal activity in extremely small dosages while others require larger dosages to be pesticidally effective. In general, the compounds of this invention that exhibit the highest order of herbicidal activity also exhibit the highest order of miticidal and mite ovicidal activity. Miticidal and/or mite ovicidal and herbicidal activity is greatest in those compounds having a hydrogen, methyl, nitro, or halogen substituent at one of the ortho positions of the 2-phenyl moiety, and a methyl or halogen group at the other position. Herbicidal activity is greatest in those compounds having, in addition to the aforementioned, ethyl and CF.sub.3 at the ortho position of the 2-phenyl moiety.

It has also been found that some of the pesticidal compositions of this invention exhibit excellent fumigant properties. In addition, these compounds are relatively non-toxic to mammals when used in amounts sufficient to kill mites, mite eggs or undesirable plant growth.

Preferred because of their higher level of miticidal and mite ovicidal activity are the 2-aryl-1,3-cyclohexanedione enol ester compounds of this invention in which:

R.sub.1, R.sub.2, R.sub.4 and R.sub.5 are individually hydrogen, methyl, halo or nitro with the proviso that when R.sub.1 is hydrogen or nitro, then R.sub.5 cannot be hydrogen or nitro;

R.sub.3 is hydrogen, methyl or halo;

R.sub.6 through R.sub.11 inclusive are individually hydrogen, C.sub.1 -C.sub.8 alkyl, CF.sub.3, unsubstituted phenyl, or

R.sub.8 and R.sub.9 together form a cyclopentyl or cyclohexyl ring.

Preferred because of their higher level of herbicidal activity are the 2-aryl-1,3-cyclohexanedione enol ester compounds of this invention in which:

R.sub.1 is ethyl;

R.sub.2 to R.sub.5 inclusive are individually hydrogen, methyl, CF.sub.3 or halogen

with the proviso that halogen atoms may not occupy adjacent positions on the aromatic ring;

R.sub.6, R.sub.7, R.sub.10 and R.sub.11 are hydrogen;

R.sub.8 and R.sub.9 are individually hydrogen, unbranched C.sub.1 -C.sub.4 alkyl, isopropyl, tertiary butyl, diethyl methyl, cycloalkyl, CF.sub.3

with the proviso that when R.sub.8 or R.sub.9 is ethyl, isopropyl, or diethyl methyl, then R.sub.14 is C.sub.1 to C.sub.4 alkyl and R is C.sub.1 C.sub.15 alkyl; or

R.sub.8 and R.sub.9 together form a cyclopentyl or cyclohexyl ring

with the proviso that when R.sub.8 and R.sub.9 together form a cyclohexyl ring, R is an unbranched C.sub.1 to C.sub.14 alkyl; and

R is

unbranched C.sub.1 to C.sub.17 alkyl, unsubstituted C.sub.3 -C.sub.6 cycloalkyl,

unbranched C.sub.1 to C.sub.6 alkyl C.sub.3 -C.sub.6 cycloalkyl, tertiary butyl,

unsubstituted or non-ortho C.sub.1 to C.sub.4 alkyl, halo, or nitro substituted phenyl, ortho-substituted C.sub.1 -C.sub.6 alkyl phenyl or ##STR4## wherein: R.sub.12 is C.sub.1 to C.sub.7 alkyl or C.sub.1 -C.sub.7 alkylene, and

R.sub.13 and R.sub.14 are individually C.sub.1 to C.sub.3 alkyl.

The 2-aryl-1,3-cyclohexandione enol ester compounds of this invention can be conveniently prepared by a variety of methods. Two preferred methods which utilize the 2-aryl-1,3-cyclohexanedione parent compound as the precursor are illustrated by the general reaction schemes set forth below in which R, R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.7, R.sub.8, R.sub.9, R.sub.10 and R.sub.11 are as described above and X is halogen, or ##STR5## except as noted: ##STR6##

In the reactions illustrated in METHOD I one equivalent of the corresponding 2-aryl-cyclohexane-1,3-dione compound is reacted with an appropriately substituted acid halide or anhydride compound in the presence of at least one equivalent of an acid acceptor, preferably in an inert solvent.

The acid acceptor utilized in the reactions of METHOD I can be either an organic or an inorganic base. Illustrative of organic bases that are useful as acid acceptors in the conduct of these reactions one can mention tertiary amines, such as triethylamine, pyridine, trimethylamine or 1,4-diazobicyclo[2.2.2] octane; or alkali metal alkoxides, as for example, sodium methoxide, sodium ethoxide or the like. Bases such as sodium carbonate, sodium hydroxide or potassium hydroxide are illustrative of inorganic bases that are useful as acid acceptors. Preferred organic acid acceptors are tertiary amines such as triethylamine, pyridine or trimethylamine.

In general, any organic solvent that is inert to the reactants or reaction conditions may be employed in the reaction of METHODS I. Illustrative of organic solvents which are generally suitable for use in the conduct of these reactions are saturated, unsaturated and aromatic hydrocarbons, e.g., hexane, cyclohexane, octane, cyclohexene, dodecane, naphtha, Decalin, kerosene, cycloheptane, benzene, toluene, xylene, naphthalene or the like; ethers such as dioxane, tetrahydrofuran, diethyl ether; tetrahydropyran, 1,2-dimethyoxybenzene, 1,2-diethyl benzene, the dialkyl ethers of ethylene glycol, of propylene glycol or chlorinated aliphatic hydrocarbons as for example, chloroform, dichloromethane, methylene dichloride, 1,1-dichloroethane, carbon tetrachloride or the like.

In a preferred embodiment, the reactions, illustrated in METHOD I are conducted in a solvent that also functions as the acid acceptor. Illustrative of such multifunctional solvents are N,N-dimethylaniline, pyridine, alpha-picoline, any lutidine, collodine or any like aromatic or heterocyclic tertiary amine compound.

The reactions illustrated in METHOD I are neither temperature nor pressure sensitive and can be conducted over a broad temperature and pressure range to yield the desired product. Preferably, these reactions are conducted at a temperature of from -40.degree. C. to about 120.degree. C. and at atmospheric or autogeneous pressure.

The acid halide, acid and anhydride compounds utilized as reactants in the procedure described in METHODS I above are known classes of compounds that can either be obtained from commercial sources or prepared in accordance with conventional methods known to those skilled in the art.

The 2-aryl-1,3-cyclohexanedione compounds utilized as reactants in the procedure of METHOD I can be conveniently prepared in accordance with a number of synthetic procedures. For example, 2-aryl-1,3-cyclohexanedione compounds in which R.sub.5 is hydrogen can be prepared by heating the corresponding 6-aryl-5ketopolyalkyl hexanoic acid compound with sulfuric acid or alternatively by treating the corresponding 6-aryl-5-ketopolyalkylhexanoic acid ester with base. The 2-aryl-cyclohexane-1,3-dione compounds in which at least one ortho substituent is alkyl and the other ortho substituent is other than hydrogen, can be conveniently prepared by the benzophenone sensitized photolysis of the corresponding 2-diazocyclohexane-1,3-dione compound in an appropriately substituted aromatic solvent. The remaining 2-aryl-1,3-cyclohexanedione precursors can be conveniently prepared by reacting the corresponding 1,3-cyclohexanedione compound with an appropriately substituted halonitrobenzene compound. These synthetic procedures are described in more detail in U.S. Pat. No. 4,209,532 entitled "BIOCIDAL 2ARYL-1,3-CYCLOHEXANE-DIONE COMPOUNDS".

The following specific examples are presented to more particularly illustrate this invention.

A solution of 1.009 (3.99 mmol) of 2-(2'-chlorophenyl)-5,5-dimethyl-1,3-cyclohexanedione and 0.03 g (8.0 mmol) of pyridine was cooled in an ice bath and stirred under N.sub.2. The 2-ethylhexanoyl chloride (0.69 g, 4.25 mmol) was added, the mixture was then allowed to warm to room temperature, stirred at room temperature for one hour and refluxed for one hour. The solvent was removed under reduced pressure and the residue taken up in ether and water. The ether was washed three times with 0.25N NaOH, three times with 10% HCl and with water. The ether was dried over anhydrous MgSO.sub.4 and decanted to give 1.23 g (82%) of 3-(2'-ethylhexanoyloxy)-2-(2'-chlorophenyl)-5,5-dimethyl-2-cyclohexenone as a clear colorless oil which was homogeneous by thin layer chromatograpy.

Calculated for C.sub.22 H.sub.29 ClO.sub.3 : C, 70.10; H, 7.76. Found: C, 70.09; H, 7.86.

A solution of 1.76 g (7.02 mmol) of 2-(2',4'-dichlorophenyl)-5,5-dimethyl-1,3-cyclohexanedione in 10 ml of chloroform was cooled in ice and 1.11 g (14.04 mmol) of pyridine added followed by 1.21 g (7.47 mmol) of 2-ethylhexanoyl chloride. The mixture was stirred for 2 hrs. at room temperature and then refluxed for 12 hours.

The reaction mixture was worked up exactly as described for Example I above to give 2.09 g of a yellow oil. This material was chromatographed using low pressure liquid chromatography on silica gel with a hexane-ethyl acetate gradient to give 1.15 g (41%) of 3-(2'-ethylhexanoyloxy)-2-(2',4'-dichlorophenyl)-5,5-dimethyl-2-cyclohexen one as a clear, colorless oil. The thin layer chromatogram (80:20 hexane-ethyl acetate) of this material showed one spot at Rf=0.46.

Calculated for C.sub.22 H.sub.28 Cl.sub.2 O.sub.3 : C, 64.23; H, 6.86. Found: C, 64.44; H, 6.80.

A solution of 1.50 g (6.14 mmol) of 2-(2',4'-dimethylphenyl)-5,5-dimethyl-1,3-cyclohexanedione in 10 ml of chloroform was cooled in ice and 1.94 g (24.56 mmol) of pyridine added followed by 1.64 g (12.28 mmol) of hexanoyl chloride. The mixture was stirred for 2 hrs. at room temperature, then refluxed for 5 hrs.

The reaction mixture was cooled to room temperature and taken up in 150 ml of ether. The ether was washed three times with 50 ml of 0.25N NaOH, twice with 50 ml portions of ice cold 6N HCl, and twice with water. The ether was dried over anhydrous (MgSO.sub.4) and removed under reduced pressure to leave 0.98 g (47% yield) 3-hexanoyloxy-5,5-dimethyl-2-(2',4'-dimethylphenyl)-2-cyclohexenone as a clear, colorless oil. This oil showed one spot on a thin layer chromatogram (70:30 hexane-ethyl acetate) at Rf=0.49.

Calculated for C.sub.22 H.sub.30 O.sub.3 : C, 77.15; H, 8.83. Found: C, 77.25; H, 8.92.

A solution of 1.50 g (6.14 mmol) of 2-(2',4'-dimethylphenyl)-5,5-dimethyl-1,3-cyclohexanedione in 10 ml of chloroform was cooled in ice and 1.94 g (24.56 mmol) of pyridine added followed by 2.00 g (12.28 mmol) of 2-ethylhexanoyl chloride. The mixture was stirred for 2 hrs. at room temperature, then refluxed for 12 hrs. The mixture was worked up exactly as described in Example I above to give 1.58 g of a slightly yellow, viscous oil. This material was chromatographed through 75 g of silica gel (0.063-0.2 mm) using a gradient ranging from 98:2 to 90:10 hexane-ethyl acetate. The chromatography gave 1.15 g (51%) of 3-(2-ethylhexanoyloxy)-5,5-dimethyl-2-(2',4'-dimethylphenyl)-2-cyclohex enone as a clear colorless oil which showed one spot on a thin layer chromatogram (70:30 hexane-ethyl acetate) at Rf=0.52.

Calculated for: C.sub.24 H.sub.34 O.sub.3 : C, 77.80; H, 9.25. Found: C, 77.34; H, 9.48.

A solution of 2.00 g (8.00 mmol) of 2-(2',4'-dichlorophenyl)-5,5-dimethyl-1,3-cyclohexanedione in 10 ml of chloroform was cooled in ice and 1.26 g (16.00 mmol) of pyridine was added followed by 1.14 g (8.50 mmol) of hexanoyl chloride. The mixture was stirred for 2 hrs. at room temperature and refluxed for 12 hrs.

The reaction mixture was worked up exactly as described for Example I above to give 1.94 g of a slightly yellow oil. This material was chromatographed using a low pressure liquid chromatography system and a hexane-ethyl acetate gradient. Work-up of the chromatography gave 1.55 g (51% yield) of 3-hexanoyloxy-2-(2',4'-dichlorophenyl)-5,5-dimethyl-2-cyclohexenone as a clear, colorless oil which on a thin layer chromatogram (80:20 hexane-ethyl acetate) showed one spot at Rf=0.27.

Calculated for C.sub.20 H.sub.24 Cl.sub.2 O.sub.3 : C, 62.67; H, 6.31. Found: C, 62.83; H, 6.32.

A suspension of 1.50 g (6.14 mmol) of 2-(2',5'-dimethylphenyl)-5,5-dimethyl-1,3-cyclohexanedione in 15 ml of dry benzene was prepared and 0.49 g (7.37 mmol) of 85% powdered potassium hydroxide was added, followed by 1 drop of dicyclohexyl-18-crown-6-ether. After stirring for 30 minutes, 1.20 g (7.37 mmol) of 2-ethyl-hexanoyl chloride was added, and the reaction mixture refluxed for 12 hours. The reaction mixture was cooled to room temperature, taken up in 150 ml ether and 50 ml of water, washed three times with 0.25N NaOH, two times with water, two times with 6N HCl, and once more with water. The ether solution was dried and stripped to leave 2.10 g (92% yield) of 3-(2-ethylhexanoyloxy)-5,5-dimethyl-2-(2',5'-dimethylphenyl)-2-cyclohexeno ne as a clear, colorless oil.

Calculated for C.sub.24 H.sub.34 O.sub.3 : C, 77.80; H, 9.25. Found: C, 77.46; H, 8.98.

A 500 ml 3-neck round bottom flask was equipped with a mechanical stirrer, addition funnel, and reflux condenser. The glassware was dried thoroughly and the flask charged with 4.62 g (0.096 g-atom) of 50% sodium hydride in mineral oil. The oil was washed off the NaH using toluene, and then 100 ml of toluene added. The mixture was warmed to 65.degree. C. and 12.62 g (0.0481 mol) ethyl 6-(2',4'-dimethylphenyl)-5-ketohexanoate added, dropwise, over a 2 hr. period. The mixture was maintained at 65.degree. C. for 12 hours, then carefully quenched with 25 ml of ice water. The reaction mixture was diluted with 250 ml of water and extracted twice with 150 ml of ether. The aqueous base solution was acidified to pH=3 with 6N HCl, and extracted twice with 150 ml of methylene chloride. The methylene chloride was washed with water, dried over anhydrous MgSO.sub.4 and stripped to give 5.88 g of a semi-solid. This was recrystallized from ethyl acetate to give 5.10 g (49%) of 2-(2',4'-dimethylphenyl)-1,3-cyclohexanedione as a white, crystalline solid, m.p. 143.degree.-145.degree. C.

Calculated for C.sub.14 H.sub.16 O.sub.2 : C, 77.75; H, 7.46. Found: C, 76.99; H, 7.46.

A 500 ml one-neck round bottom flask was charged with 10.0 g (0.0416 mol) of 6-(2'-chlorophenyl)-5-ketohexanoic acid and 100 ml of 72% sulfuric acid. The reaction mixture was stirred and heated to 120.degree. C. for 51/2 hrs. (oil bath) then poured into 600 ml of ice water. A tacky, white solid formed, and this was extracted into 300 ml of methylene chloride. The CH.sub.2 Cl.sub.2 solution was washed six times with water, dried over anhydrous MgSO.sub.4, and stripped to leave 8.87 g of a tacky, white solid. This material was recrystallized from ethyl acetate to give 5.85 g (63%) of 2-('-Chlorophenyl)-1,3-cyclohexanedione as a white, crystalline solid, m.p. 148.5.degree.-149.degree. C.

Calculated for C.sub.12 H.sub.11 ClO.sub.2 : C, 64.73; H, 4.98. Found: C, 64.49; H, 4.89.

A solution containing 42.05 g (0.300 mol) of 5,5-dimethyl-1,3-cyclohexanedione and 100 g (0.718 g-atom) of anhydrous potassium carbonate in 300 ml of dry dimethylformamide was heated to 75.degree. C. under nitrogen and stirred for one hour. The 3,4-dichloronitrobenzene, 57.60 g (0.300 mol) was dissolved in 100 ml of dimethylformamide and added dropwise to the reaction mixture while stirring and maintaining the temperature of the reaction mixture at 75.degree. C. A deep red-colored solution formed, and when the addition was complete the reaction temperature was raised to 100.degree. C. and held at this temperature for 3 hours. Most of the dimethylformamide was removed by vacuum distillation. The residue was poured into 2 L of ice water and extracted three times with 500 ml of benzene. Nitrogen was then passed through the aqueous solution while warming to remove dissolved benzene. The aqueous solution was cooled in an ice bath and acidified to give a tacky precipitate, which, upon warming solidified and was collected by suction filtration. The reaction product was recrystallized from acetone to give 31.7 g (36%) of 2-(2'-Chloro-4'-nitrophenyl)-5,5-dimethyl-1,3-cyclohexanedione as a white power, m.p. 250.degree.-253.degree. C.

Calculated for: C.sub.14 H.sub.14 Cl NO.sub.4.1/2H.sub.2 O: C, 55.18; H, 4.96; N, 4.60. Found: C, 55.53; H, 4.73; N, 5.09.

A solution of 20.0 g (0.067 mol) of 2-(2'-chloro-4'-nitrophenyl)-5,5-dimethyl-1,3-cyclohexanedione in 150 ml of concentrated ammonium hydroxide and 150 ml of ethanol was stirred at room temperature while passing hydrogen sulfide gas through the solution at such a rate that all of the H.sub.2 S was absorbed. When the solution was saturated with H.sub.2 S, the temperature was raised to the reflux point and H.sub.2 S continuously passed slowly through the refluxing solution for 24 hours. The reaction mixture was filtered to remove sulfur, then the filtrate evaporated under reduced pressure. To the residue was added 300 ml of 0.25N NaOH, and the solution filtered once more. The filtrate was collect and carefully acidified to pH=4 with 6N HCl. A white solid formed which was collected by suction filtration to give 13.3 g (74%) of 2-(2'-Chloro-4'-aminophenyl)-5,5-dimethyl-1,3-cyclohexanedione, m.p. 218.degree.-19.degree. C.

Calculated for: C.sub.14 H.sub.16 Cl NO.sub.2.1/2H.sub.2 O: C, 61.20; H, 6.24; N, 5.10. Found: C, 60.44; H, 5.83; N, 5.32.

The 2-(2'-chloro-4'-aminophenyl)-5,5-dimethyl-1,3-cyclohexanedione (9.66 g. 0.0364 mol) was added to 7.0 ml of concentrated HCl in 150 ml of water, and the mixture stirred and heated almost to boiling. An additional 15.0 ml of HCl was added and the mixture cooled to 0.degree.-5.degree. C. A solution of 3.22 g (0.0467 mol) of sodium nitrite in 9.0 ml of water was added dropwise while the reaction mixture was stirred and maintained at 0.degree.-5.degree. C. When addition of the sodium nitrite solution was complete, the reaction mixture was stirred at 0.degree.-5.degree. C. for one hour.

The diazonium salt solution prepared above was added in portions to 161 ml of 50% hypophosphorous acid at 0.degree. C., with stirring and cooling. The reaction mixture was stirred for 12 hours and filtered to give 8.55 g of a tan solid. This material was chromatographed through 250 g of Woelm silica gel (0.063-0.2 mm) eluting with a gradient from pure benzene to 70:30 benzene-ethyl acetate. A total of 7.12 g of product was obtained from the chromatography and recrystallized from benzene-ethyl acetate to give 6.85 g (75%) of 2-(2'-Chlorophenyl)-5,5-dimethyl-1,3-cyclohexanedione as white crystals, m.p. 191.degree.-192.degree. C.

Calculated for: C.sub.14 H.sub.15 C.sub.1 O.sub.2 : C, 67.07; H, 6.03. Found: C, 67.04; H, 6.00.

A solution of 5.00 g (0.036 mol) of 2-diazocyclohexane-1,3-dione in 500 ml of mesitylene (dry, distilled) containing 32.8 g (0.18 mol) benzophenone was degassed with nitrogen for one hour, and irradiated with a 200 watt Hanovia immersion lamp through a borosilicate glass filter, until the complete disappearance of the diazo band (4.68 u) in the infrared was observed. The reaction was also monitored by thin layer chromatography (90:10 ethyl acetate-benzene) and irradiation continued until no diazoketone at R.sub.f =0.31 could be seen. The irradiation required 11 hours. The mesitylene was extracted with 0.25N sodium hydroxide until a small aliquot showed no cloudiness upon acidification. The combined base extracts were washed twice with 200 ml of ether, and acidified (pH=5) with 1N HCl. The aqueous solution was extracted three times with 75 ml portions of chloroform, dried over anhydrous MgSO.sub.4, and the solvent stripped to give 5.06 g of a tan solid.

This solid was chromatographed through 250 g of silica gel (0.063-0.2 mm) eluting with a gradient from pure benzene to 80:20 benzene-ethyl acetate. A total of 2.60 g (31%) of a white solid (honogeneous by thin layer chromatography) was obtained and recrystallized from diisipropyl ether to give 1.96 g of 2-(2',4',6'-trimethylphenyl)-1,3-cyclohexanedione as white crystals, mp 196.degree.-198.degree. C.

Calculated for: C.sub.15 H.sub.18 O.sub.2 : C, 78.23; H, 4.88. Found: C, 77.94; H, 8.20.

Selected 2-aryl-1,3-cyclohexanedione enol ester compounds representative of those useful in accordance with this invention were tested with respect to their miticidal, mite ovidical and pre-emergent and post-emergent herbicidal activity.

Suspensions of the test compounds were prepared by dissolving one gram of compound in 50 milliliters of acetone in which had been dissolved 0.1 gram (10 percent of the weight of compound) of an alkyl-phenoxyethanol surfactant, as an emulsifying or dispersing agent. The resulting solution was mixed into 160 milliliters of water to give roughly 200 milliliters of a suspension containing the compound in finely divided form. The thus prepared stock suspension contained 0.5 percent by weight of compound. The test concentrations employed in the tests described hereinbelow were obtained by diluting the stock suspension with water. The test procedures were as follows:

Adults and nymphal stages of the two-spotted mite (tetranychus uriticae (Koch)), reared on Tendergreen bean plants at 80.+-.5.degree. F., and 50.+-.5.degree. percent relative humidity, were the test organisms. Infested leaves from a stock culture were placed on the primary leaves of two bean plants six to eight inches in height, growing in a two-and-a-half inch clay pot. 150-200 Mites, a sufficient number for testing, transferred from the excised leaves to the fresh plants in a period of twenty-four hours. Following the twenty-four hour transfer period, the excised leaves were removed from the infested plants. The test compounds were formulated by diluting the stock suspension with water to provide suspensions containing 500 parts of test compound per million parts of final formulation. The potted plants (one pot per compound) were placed on a revolving turntable and sprayed with 100-110 milliliters of test compound formulation by use of a DeVilbis spray gun set at 40 psi. air pressure. This application, which lasted 30 seconds, was sufficient to wet the plants to run-off. As a control, 100-110 milliliters of a water solution containing acetone and emulsifier in the same concentrations as the test compound formulation, but containing no test compound, were also sprayed on infested plants. The sprayed plants were held at 80.+-.5.degree. F. and 50.+-.5 percent relative humidity for four days, after which, a mortality count of motile forms was made. Microscopic examination for motile forms was made on the leaves of the test plants. Any individual which was capable of locomotion upon prodding was considered living.

The test organism was the egg of the two-spotted mite (Tetranychus uriticae (Koch)), as obtained from adults reared on Tendergreen bean plants under controlled conditions of 80.+-.5.degree. F. and 50.+-.5 percent relative humidity. Heavily infested leaves from a stock culture were placed on the primary leaves of two bean plants six to eight inches in height, growing in a two-and-a-half inch clay pot. Females were allowed to oviposit for a period of 48 hours and then the leaves of the infested plants were dipped in a solution containing 800 parts of tetraethyl pyrophosphate per million parts of water in order to destroy the reproductory forms and thus prevent further egg laying. This solution of tetraethyl pyrophosphate does not affect the viability of the eggs. The plants were allowed to dry thoroughly. The test compounds were formulated by diluting the stock suspension with water to give a suspension containing 500 parts of test compound per million parts of final formulation. The potted plants (one pot per compound) were placed on a revolving turntable and sprayed with 100-110 milliliters of test compound formulation by use of a DeVilbis spray gun set at 400 psig. air pressure. This application, which lasted 30 seconds, was sufficient to wet the plants to run-off. As a control, 100-110 milliliters of a water solution containing acetone and emulsifier in the same concentrations as the test compound formulation, but containing no test compound, were also sprayed on plants infested with eggs. The sprayed plants were held at 80.+-.5.degree. F. and 50.+-.5 percent relative humidity for four days, after which a microscopic examination was made of unhatched (dead) and hatched (living) eggs.

In these tests the pesticidal activity of the compounds against mites and mite eggs was rated as follows:

A=Excellent Control

B=Partial Control

C=No Control

The following seeds were used in this test:

Perennial rye grass--Solium perenne

Crabgrass--Sigitaria sanguinalis

Red root pigweed--Amaranthus retroflexus

Mustard--Brassica pncia var. foliosa (Florida broadleaf)

Two seed-soil mixtures were prepared as follows:

Mixture I

196 cc. Rye grass seed

75 cc. Amaranthus

18,000 cc. Sifted, fairly dry soil

Mixture II

99 cc. Crabgrass seed

33 cc. Amaranthus

18,000 cc. Sifted, fairly dry soil

Each of the above mixtures was rolled separately in 5 gallon containers for approximately one-half hour on a ball mill to insure uniform mixing of seeds and soil. For each compound four 3-inch pots were filled with soil to within 11/2 inches of the top of the pots. To two of these pots was added 70 cc. of Mixture I. To the remaining two pots was added 70 cc. of Mixture II. The seed-soil mixture was tamped firmly, and the pots were removed to the greenhouse and watered lightly. About 2 hours after planting, 25 milliliters of the test formulation were added to each of two pots for each soil-seed mixture; i.e., one replicate of each seed mixture per concentration. An equal volume of a water solution containing acetone and an emulsifier in the same concentration as the herbicidal mixture but without the candidate herbicide was also added to each of the soil-seed mixtures. These pots are used as as check or control units. The test compounds are formulated by standard procedure of solution in acetone, addition of an emulsifier, and dilution with water. Tests were conducted on all compositions at low concentration (100 ppm.). Certain compositions were also tested at high concentration (1000 ppm). The pots were held in the greenhouse and watered lightly until results were taken. Ten to twelve days after application of chemical, injury is noted for each species by comparing treated vs. untreated pots. Ratings are made at both the high and the low concentrations (1000 ppm and 100 ppm) according to the following designations:

5=no seedlings emerged

4=few seedlings emerged and/or very severe stunting

3=moderate reduction in stand and/or moderate stunting

2=very slight reduction in stand and/or slight stunting

1=no injury; seedlings appear no different with respect to stand and/or growth than untreated controls

Experiments were also conducted to determine the phytotoxicity of representative compositions with respect to healthy fresh plants. Solutions of the compounds were prepared as described above to provide a concentration of 2500 parts per million of the test compound. The test plants were sprayed in accordance with the procedure described above for the Mite Foliage Spray Test so as to deliver approximately 100 milliliters of test solution to the leaves of each plant tested. The sprayed plants and controls were set aside for approximately one hour to allow the solutions to dry and were then placed in the greenhouse. After ten days the plants were visually inspected to determine the extent of foliage injury. A rating of 1 indicates no perceptible injury; 5 indicates the plant was dead and ratings of 2, 3 and 4 indicate intermediate degrees of injury based upon the number and extent to which leaves were injured.

The results of these experiments are summarized and set forth in Tables I and II below. Physical Properties and Miticidal Activity of 2-Aryl-1,3-Cyclohexanedion e Enol Ester Compounds ##STR7## Miticidal Elemental Analysis Activity EX R R.sub.1 R.sub.2 R.sub.3 R.sub.4 R.sub.5 R.sub.6 R.sub.7 R.sub.8 R.sub.9 R.sub.10 R.sub.11 M.P. .degree.C.; and/or IR Adult Egg 1 ##STR8## Cl H Cl H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.); 5.75(ester CO); 6.05(KETO CO) A A 2 (CH.sub.2).sub.6 CH(CH.sub.3).sub.2 Cl H Cl H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.70 A A (ester CO); 5.75, 6.0 (KETO CO) 3 ##STR9## Cl H Cl H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.75(ester CO); 6.0 6.05(KETO CO) A A 4 (CH.sub.2).sub.16 CH.sub.3 Cl H Cl H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.75 A A (ester CO); 6.05 (KETO CO) 5 ##STR10## Cl H Cl H H H H CH.sub.3 CH.sub.3 H H 76.5-78.0 A A 6 C(CH.sub.3).sub.3 Cl H Cl H H H H CH.sub.3 CH.sub.3 H H 91.0-93.0 A A 7 (CH.sub.2).sub.4 CH.sub.3 Cl H Cl H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.70 A A (ester CO); 6.0, 6.05 (KETO CO) 8 ##STR11## Cl H Cl H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.70(ester CO); 6.0, 6.05(KETO CO) A A 9 CH.sub.3 Cl H H H Cl H H CH.sub.3 CH.sub.3 H H 41.0-42.5 A A 10 C(CH.sub.3).sub.3 Cl H H H Cl H H CH.sub.3 CH.sub.3 H H 84-85 A A 11 CH.sub.3 Cl H Cl H Cl H H CH.sub.3 CH.sub.3 H H 99.5-101 A A 12 (CH.sub.2).sub.4 CH.sub.3 Cl H H H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.72 A A (ester CO; 6.0, 6.05 (KETO CO) 13 ##STR12## Cl H H H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.70(ester CO); 5.95, 6.0(KETO CO) A A 14 ##STR13## Cl H H H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.68(ester CO); 5.95, 6.0(KETO CO) A A 15 (CH.sub.2).sub.6 CH(CH.sub.3).sub.2 Cl H H H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.75 A A (ester CO); 6.0, 6.05 (KETO CO) 16 ##STR14## Cl H H H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.75(ester CO); 6.0, 6.05(KETO CO) A A 17 (CH.sub.2).sub.16 CH.sub.3 Cl H H H H H H CH.sub.3 CH.sub.3 H H 47-49 A A 18 CH.sub.3 Cl H Cl H H H H CH.sub.3 CH.sub.3 H H 92.5-94 A A 19 CH(CH.sub.3).sub.2 Cl H Cl H H H H CH.sub.3 CH.sub.3 H H 65.5-66.5 A A 20 CH.sub.3 Cl H H H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.70 A A (ester CO); 6.05 (KETO CO) 21 CH(CH.sub.3).sub.2 Cl H H H H H H CH.sub.3 CH.sub. 3 H H .lambda.max (.mu.): 5.73 A A (ester CO); 6.05 (KETO CO) 22 ##STR15## Cl H H H H H H CH.sub.3 CH.sub.3 H H 77-78 A A 23 C(CH.sub.3).sub.3 Cl H H H H H H CH.sub.3 CH.sub.3 H H 86-87 A A 24 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.75 A A (ester CO); 6.05, 6.10 (KETO CO) 25 CH(CH.sub.3).sub .2 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H 238-240 A A 26 CH.sub.3 CH.sub.3 H H H NO.sub.2 H H CH.sub.3 CH.sub.3 H H 79.5-81 A A 27 C(CH.sub.3).sub.3 CH.sub.3 H H H NO.sub.2 H H CH.sub.3 CH.sub.3 H H 101.5-103 A A 28 CH.sub.3 Cl H H H H H H H H H H .lambda.max (.mu.): 5.70 C A (ester CO); 6.10 (KETO CO) 29 (CH.sub.2).sub.4 CH.sub.3 Cl H H H H H H H H H H .lambda.max (.mu.): 5.70 A A (ester CO); 6.00, 6.05 (KETO CO) 30 ##STR16## Cl H H H H H H H H H H .lambda.max (.mu.): 5.72(ester CO); 6.00, 6.10(KETO CO) A A 31 (CH.sub.2).sub.16 CH.sub.3 Cl H H H H H H H H H H .lambda.max (.mu.): 5.72 C A (ester CO); 6.00, 6.10 (KETO CO) 32 (CH.sub.2).sub.4 CH.sub.3 Cl H Cl H H H H H H H H .lambda.max (.mu.): 5.70 A A (ester CO); 5.98, 6.08 (KETO CO) 33 CH(CH.sub.3).sub.2 CH.sub.3 H H H H H H H H H H .lambda.max (.mu.): 5.73 A A (ester CO); 6.03, 6.12 (KETO CO) 34 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H H H H H H H H H H .lambda.max (.mu.): 5.70 A B (ester CO); 6.00, 6.08 (KETO CO) 35 (CH.sub.2).sub.16 CH.sub.3 CH.sub.3 H H H NO.sub.2 H H CH.sub.3 CH.sub.3 H H 62-63 A A 36 CH(CH.sub.3).sub.2 CH.sub.3 H H H H H H H H H H .lambda.max (.mu.): 5.75 A A (ester CO); 6.03, 6.12 (KETO CO) 37 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H H H H H H H H H H .lambda.max (.mu.): 5.70 A A (ester CO); 6.00, 6.08 (KETO CO) 38 ##STR17## Cl H Cl H H H H H H H H .lambda.max (.mu.): 5.70(ester CO); 5.98, 6.08(KETO C O) A A 39 (CH.sub.2).sub.16 CH.sub.3 Cl H Cl H H H H H H H H 34.0-34.5 A A 40 ##STR18## CH.sub.3 H CH.sub.3 H H H H H H H H .lambda.max (.mu.): 5.75(ester CO); 6.00, 6.10(KETO CO) A A 41 (CH.sub.2).sub.16 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H H H H H .lambda.max (.mu.): 5.75 A A (ester CO); 6.00, 6.15 (KETO CO) 42 ##STR19## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.78(ester CO); 6.05, 6.15(KETO CO) A A 43 ##STR20## Cl H CH.sub.3 Cl H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.78(ester CO); 6.05, 6.10(KETO CO) A A 44 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H H CH.sub.3 H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.) 5.75 A A (ester CO); 6.00, 6.05 (KETO CO) 45 ##STR21## CH.sub.3 H H CH.sub.3 H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.) 5.75(ester CO); 6.05, 6.10(KETO CO) A A 46 CH.sub.3 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.) 5.70 A A (ester O C); 6.00, 6.05 (KETO CO) 47 CH(CH.sub.3).sub.2 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H 77-78 A A 48 ##STR22## CH.sub.3 H H H H H H H H H H .lambda.max (.mu.): 5.78(ester CO); 6.00, 6.10(KETO CO) A A 49 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H H H H H .lambda.max (.mu.): 5.73 A A (ester CO); 6.00, 6.10 (KETO CO) 50 (CH.sub.2).sub.16 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.75 A A (ester CO); 6.05, 6.10 (KETO CO) 51 CH(CH.sub. 3).sub.2 CH.sub.3 H H CH.sub.3 H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.) 5.80 A B (ester CO); 6.10, 6.15 (KETO CO) 52 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H CH.sub.3 CH.sub.3 H H 110-111 A A 53 (CH.sub.2).sub.16 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H CH.sub.3 CH.sub.3 H H 29-30 A A 54 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H .lambda.max (.mu.): 5.78 A A (ester CO); 6.05, 6.15 (KETO CO) 55 C(CH.sub.3).sub.3 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H 79-84 A A 56 C(CH.sub.3).sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H H H H 132-133 C A 57 (CH.sub.2).sub.16 CH.sub.3 CH.sub.3 H H H H H H H H H H 38-40 A A 58 C(CH.sub.3).sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H H H H 71-73 B B 59 C(CH.sub.3).sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H CH.sub.3 CH.sub.3 H H 61-62 A A 60 C(CH.sub.3).sub.3 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.16 8.83 Found 77.28 8.87 61 ##STR23## H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H Calc.Found C77.2777.49 H 8.037.91 A A 62 CH(C.sub.2 H.sub.5).sub.2 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.49 9.05 Found 77.83 9.22 63 C(CH.sub.3).sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.49 9.05 Found 77.25 9.13 64 ##STR24## CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H Calc.Found 7 C7.6177.63 H 8.298.32 A A 65 CH(C.sub.2 H.sub.5).sub.2 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.80 9.25 Found 78.18 9.41 66 CHC(CH.sub.3).sub.2 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.93 8.53 Found 77.89 8.65 67 (CH.sub.2).sub.14 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 79.79 10.55 Found 80.45 10.80 68 (CH.sub.2).sub.7 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 78.35 9.61 Found 78.51 9.80 69 (CH.sub.2).sub.10 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 79.04 10.06 Found 79.07 10.34 70 (CH.sub.2).sub.7 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 78.60 9.77 Found 79.10 10.01 71 (CH.sub.2).sub.10 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 79.25 10.29 Found 79.57 10.45 72 (CH.sub.2).sub.4 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CH.sub.2 CH(CH.sub.3).sub.2 H H C H A A Calc. 77.80 9.25 Found 78.30 9.42 73 (CH.sub.2).sub.4 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CF.sub.3 H H C H A A Calc. 65.96 6.59 Found 65.97 6.66 74 CHC(CH.sub.3).sub.2 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.61 8.29 Found 77.96 8.45 75 (CH.sub.2).sub.3 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H CH.sub.3 CH(CH.sub.3 ).sub.2 H H C H A A Calc. 77.49 9.05 Found 77.78 9.16 76 (CH.sub.2).sub.3 CH.sub.3 H H Cl H Cl H H CH.sub.3 CH(CH.sub.3).sub.2 H H C H A A Calc. 63.43 6.59 Found 64.11 6.79 77 C.sub.2 H.sub.5 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 76.80 8.59 Found 76.68 8.66 78 CH.sub.2 CH.sub.2 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.16 8.83 Found 77.56 8.96 79 CH(CH.sub.3).sub.2 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub. 2 H H C H A A Calc. 77.16 8.83 Found 77.70 8.97 80 (CH.sub.2).sub.3 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.49 9.05 Found 77.01 9.22 81 (CH.sub.2).sub.6 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 78.35 9.61 Found 78.50 9.70 82 ##STR25## CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H Calc.Found 7 C9.7679.64 H 7.50 7.52 A A 83 C.sub.2 H.sub.5 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 76.40 8.34 Found 76.76 8.44 84 CH.sub.2 CH.sub.2 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 76.79 8.59 Found 77.04 8.43 85 CH(CH.sub.3).sub.2 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 76.79 8.59 Found 76.40 8.67 86 (CH.sub.2).sub.3 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.16 8.83 Found 77.03 8.96 87 (CH.sub.2).sub.6 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 78.08 9.44 Found 77.93 9.43 88 ##STR26## H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H Calc.Found C79.5379.57 H 7.23 7.21 A A 89 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H H H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.49 9.05 Found 77.90 9.09 90 CH(CH.sub.2 CH.sub.3).sub.2 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 76.79 8.59 Found 76.65 8.39 91 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H 47-50 A A 92 (CH.sub.2).sub.6 CH.sub.3 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 77.49 9.05 Found 78.27 8.95 93 (CH.sub.2).sub.14 CH.sub.3 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H 36-38 A A 94 (CH.sub.2).sub.16 CH.sub.3 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 77.79 10.55 Found 79.81 10.62 95 ##STR27## CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H 122-123 A A 96 CH(CH.sub.2 CH.sub.3).sub.2 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 77.15 8.83 Found 77.21 8.54 97 C(CH.sub.3).sub.2 CH.sub.2 Cl CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H 125-127 A A 98 (CH.sub.2).sub.6 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 77.80 9.25 Found 78.55 9.29 99 (CH.sub.2).sub.8 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 78.35 9.61 Found 79.18 9.79 100 C(CH.sub.3).sub.2 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 78.35 9.61 Found 79.90 9.62 101 (CH.sub.2).sub.14 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 79.62 10.44 Found 80.64 10.62 102 ##STR28## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H 61-62 A A 103 ##STR29## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H 82-84 A A 104 ##STR30## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H 113-115 A A 105 ##STR31## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H 98-100 A A 106 ##STR32## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H 120-122 A A 107 ##STR33## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H 80.0-82.5 B A 108 ##STR34## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H 124-126 A A 109 ##STR35## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H Calc.Found C73.8773.04 H 7.12 6.98 B A 110 ##STR36## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H Calc.Found C80.3480.61 H 8.19 8.08 A A 111 ##STR37## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H Calc.Found C77.3976.48 H 7.89 7.81 B A 112 (CH.sub.2).sub.3 CH.sub.3 Cl H Cl H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 61.80 6.01 Found 61.46 5.93 113 (CH.sub.2).sub.5 CH.sub.3 Cl H Cl H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 63.16 7.07 Found 63.66 6.47 114 ##STR38## Cl H Cl H H H H CH CH.sub.3 H H Calc.Found C63.8064.00 H 6.12 5.94 A A 115 (CH.sub.2).sub.6 CH.sub.3 Cl H Cl H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 64.23 6.86 Found 64.43 6.74 116 (CH.sub.2).sub.8 CH.sub.3 CH.sub.3 H H CH.sub.3 H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 78.35 9.61 Found 78.60 9.77 117 (CH.sub.2).sub.6 CH.sub.3 CH.sub.3 H H CH.sub.3 H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 77.80 9.25 Found 78.43 9.22 118 ##STR39## CH.sub.3 H CH.sub.3 H CH.sub.3 H H CH.sub.3 CH.sub.3 H H Calc.Found C78.0878.48 H 9.44 9.45 A A 119 ##STR40## CH.sub.3 H CH.sub.3 H CH.sub.3 H H CH.sub.3 CH.sub.3 H H Calc.Found C78.9878.51 H 9.33 9.13 A A 120 ##STR41## CH.sub.3 H CH.sub.3 H H H CH.sub.3 H H H H Calc.Found C77.4977.96 H 9.05 9.09 A A 121 CH.sub.3 CH.sub.3 H CH.sub.3 H H H CH.sub.3 H H H H C H A A Calc. 75.25 7.06 Found 74.60 7.02 122 ##STR42## CH.sub.3 H CH.sub.3 H H CH.sub.3 CH.sub.3 H H H H 135-136 B B 123 ##STR43## CH.sub.3 H CH.sub.3 H H CH.sub.3 CH.sub.3 H H H H Calc.Found C77.8078.17 H 9.25 9.16 A A 124 ##STR44## Cl H H H H CH.sub.3 CH.sub.3 H H H H Calc.Found C70.1070.30 H 7.76 7.72 B B 125 ##STR45## Cl H H H H CH.sub.3 CH.sub.3 H H H H 96.0-97.5 B B 126 ##STR46## Cl H H H H CH.sub.3 CH.sub.3 H H H H Calc.Found C67.8868.25 H 7.68 7.64 B A 127 ##STR47## Cl H Cl H H CH.sub.3 CH.sub.3 H H H H Calc.Found C64.2364.56 H 6.86 6.69 A A 128 ##STR48## Cl H Cl H H CH.sub.3 CH.sub.3 H H H H 122-123 B B 129 ##STR49## CH.sub.3 H H H H H H H CH.sub.3 H H Calc.Found C77.1677.33 H 8.83 8.62 A A 130 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H H CH.sub.3 H H C H A A Calc. 74.97 7.40 Found 73.77 7.70 131 CH.sub.2 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H H CH.sub.3 H H C H A A Calc. 75.50 7.74 Found 74.00 7.71 132 CH(CH.sub.3).sub.2 CH.sub.3 H CH.sub.3 H H H H H CH.sub.3 H H C H A A Calc. 75.97 8.05 Found 74.56 7.87 133 (CH.sub.2).sub.3 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H H CH.sub.3 H H C H A A Calc. 76.40 8.33 Found 75.94 8.53 134 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H H CH.sub.3 H H C H A A Calc. 76.79 8.59 Found 74.84 9.56 135 ##STR50## CH.sub.3 H CH.sub.3 H H H H H CH.sub.3 H H Calc.Found C77.6175.04 H 8.29 8.35 A A 136 ##STR51## CH.sub.3 H CH.sub.3 H H H H H CH.sub.3 H H Calc.Found C77.4977.85 H 9.05 8.99 A A 137 (CH.sub.2).sub.6 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H H CH.sub.3 H H C H A A Calc. 77.49 9.05 Found 76.18 7.66 138 (CH.sub.2).sub.8 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H H CH.sub.3 H H C H A A Calc. 78.08 9.44 Found 77.23 9.60 139 ##STR52## CH.sub.3 H CH.sub.3 H H H H H CH.sub.3 H H Calc.Found C79.1276.58 H 6.63 6.54 A A 140 ##STR53## Cl H H H H H H H CH.sub.3 H H Calc.Found C69.5169.75 H 7.50 7.24 A A 141 ##STR54## Cl H H H H H H H CH.sub.3 H H Calc.Found C70.4967.50 H 5.03 5.04 A A 142 CH(CH.sub.3).sub.2 CH.sub.3 H H H H H H H C.sub.6 H.sub.5 H H 82-83.5 C A 143 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H H C.sub.6 H.sub.5 H H C H A A Calc. 79.02 6.63 Found 79.13 6.54 144 ##STR55## CH.sub.3 H CH.sub.3 H H H H H C.sub.6 H.sub.5 H H Calc.Found C80.3580.77 H 8.19 8.21 A A 145 ##STR56## CH.sub.3 H H CH.sub.3 H H H CH.sub. 3 C.sub.2 H.sub.5 H H Calc.Found C78.0878.58 H 9.44 9.24 A A 146 ##STR57## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 C.sub.2 H.sub.5 H H Calc.Found C78.0877.05 H 9.44 7.29 A A 147 ##STR58## Cl H H H H H H CH.sub.3 C.sub.2 H.sub.5 H H Calc.Found C70.6670.83 H 7.99 7.87 A A 148 ##STR59## CH.sub.3 H H H H H H CH.sub.3 C.sub.2 H.sub.5 H H Calc.Found C77.8077.76 H 9.25 9.28 A A 149 ##STR60## CH.sub.3 H H H H H H CH.sub.3 C.sub.2 H.sub.5 H H 78-80 A A 150 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H C.sub.2 H.sub.5 C.sub.2 H.sub.5 H H C H A A Calc. 76.40 8.34 Found 76.43 8.22 151 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H C.sub.2 H.sub.5 C.sub.2 H.sub.5 H H C H A A Calc. 77.80 9.25 Found 78.45 9.19 152 ##STR61## CH.sub.3 H CH.sub.3 H H H H C.sub.2 H.sub.5 C.sub.2 H.sub.5 H H Calc.Found C78.3579.13 H 9.61 9.63 A A 153 (CH.sub.2).sub.8 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H C.sub.2 H.sub.5 C.sub.2 H.sub.5 H H C H A A Calc. 78.83 9.92 Found 79.44 9.45 154 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.2 H H C H A A Calc. 76.40 8.34 Found 77.32 8.36 155 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.2 H H C H A A Calc. 77.80 9.25 Found 77.78 9.28 156 ##STR62## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.2 H H F Calc.ound C78.3578.64 H 9.61 9.64 A A 157 (CH.sub.2).sub.8 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.2 H H C H A A Calc. 78.83 9.42 Found 79.00 10.01 158 ##STR63## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.2 H H F Calc.ound C79.9579.32 H 7.50 7.54 A A 159 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.4 H H C H A A Calc. 77.15 8.33 Found 77.50 8.85 160 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.4 H H C H A A Calc. 78.35 9.61 Found 78.21 9.47 161 ##STR64## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.4 H H F Calc.ound C78.8278.35 H 9.92 9.78 B A 162 (CH.sub.2).sub.14 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.4 H H C H A A Calc. 80.24 10.85 Found 79.93 10.73 163 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 C.sub.6 H.sub.5 H H C H B A Calc. 79.28 6.94 Found 79.00 7.10 164 CH.sub.2 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 C.sub.6 H.sub.5 H H C H A A Calc. 79.53 7.23 Found 79.37 7.04 165 C(CH.sub.3).sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 C.sub.6 H.sub.5 H H C H A A Calc. 79.97 7.74 Found 79.60 7.77 166 ##STR65## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 C.sub.6 H.sub.5 H H Calc.Found C80.5280.65 H 8.39 8.18 A A 167 (CH.sub.2).sub.6 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 C.sub.6 H.sub.5 H H C H A A Calc. 80.52 8.39 Found 81.01 8.35 168 CH.sub.3 CH.sub.3 H H H H H H ##STR66## H H Calc.Found C76.4877.63 H 7.48 7.16 A A 169 CH(CH.sub.2 CH.sub.3).sub.2 CH.sub.3 H H H H H H ##STR67## H H Calc.Found C77.9377.26 H 8.53 8.45 A A 170 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H H H H H H ##STR68## H H Calc.Found C77.9378.28 H 8.53 8.36 A A 171 ##STR69## CH.sub.3 H H H H H H ##STR70## H H Calc.Found C78.4978.54 H 8.96 8.90 A A 172 (CH.sub.2).sub.8 CH.sub.3 CH.sub.3 H H H H H H ##STR71## H H Calc.Found C78.9879.39 H 9.33 9.30 A A 173 ##STR72## CH.sub.3 H H H H H H ##STR73## H H 127-129 A A 174 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H ##STR74## H H Calc.Found C76.8976.81 H 7.74 7.55 A A 175 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H ##STR75## H H Calc.Found C78.2278.68 H 8.75 8.75 A A 176 ##STR76## CH.sub.3 H CH.sub.3 H H H H ##STR77## H H Calc.Found C78.7579.03 H 9.15 9.17 A A 177 (CH.sub.2).sub.8 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H ##STR78## H H Calc.Found C79.2080.19 H 9.50 9.30 A A 178 ##STR79## CH.sub.3 H CH.sub.3 H H H H ##STR80## H H 76-78 A A 179 ##STR81## CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H Calc.Found C76.4075.52 H 8.33 8.54 A A 180 CH.sub.2 CH(CH.sub.3).sub.2 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 76.40 8.33 Found 75.85 8.10 181 ##STR82## CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H Calc.Found C76.8075.75 H 8.59 8.45 A A 182 CH.sub.2 CH(CH.sub.3).sub.2 CH.sub.3 H CH.sub.3 H H H H CH.sub.3 CH.sub.3 H H C H A A Calc. 76.80 8.59 Found 75.52 8.38 183 CH.sub.3 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.4 H H C H A A Calc. 76.79 8.59 Found 76.14 8.32 184 ##STR83## CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.4 H H Calc.Found 7 C8.5979.17 H 9.77 9.98 A C 185 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.4 H H C H A A Calc. 78.08 9.44 Found 78.54 9.56 186 (CH.sub.2).sub.14 CH.sub.3 CH.sub.3 H H H H H H CH.sub.3 CH.sub.3 (CH.sub.2).sub.4 H H C H B B Calc. 80.10 10.76 Found 80.42 10.43 187 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H ##STR84## H H Calc.Found C78.4978.84 H 8.96 8.85 A A 188 (CH.sub.2).sub.14 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H ##STR85## H H Calc.Found C80.4180.56 H10.4110.38 A A 189 ##STR86## CH.sub.3 H CH.sub.3 H H H H ##STR87## H H Calc.Found C78.9879.44 H 9.33 9.42 A A 190 CH.sub.3 CH.sub.3 H CH.sub.3 H H H H ##STR88## H H Calc.Found C77.2776.15 H 8.03 7.90 A A 191 CH(CH.sub.3).sub.2 H H C H.sub.3 Cl Cl H H CH.sub.3 CH.sub.3 H H C H A A Calc. 62.81 6.00 Found 61.94 5.98 192 ##STR89## H H CH.sub.3 Cl Cl H H CH.sub.3 CH.sub.3 H H Calc.Found C64.9465.05 H 7.11 6.87 A A 193 CH.sub.3 H H CH.sub.3 Cl Cl H H CH.sub.3 CH.sub.3 H H 89-90 A B 194 (CH.sub.2).sub.6 CH.sub.3 H H CH.sub.3 Cl Cl H H CH.sub.3 CH.sub.3 H H C H A A Calc. 64.94 7.11 Found 65.27 6.80 195 (CH.sub.2).sub.4 CH.sub.3 H H CH.sub.3 Cl Cl H H H CH.sub.3 H H C H A B Calc. 62.67 6.32 A B Found 63.12 6.44 196 CH.sub.3 H H CH.sub.3 Cl Cl H H H CH.sub.3 H H C H C B Calc. 58.73 4.93 Found 58.69 4.88 197 ##STR90## H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H Calc.Found C78.0878.86 H 9.44 9.47 A A 198 CH.sub.3 H H Cl H Cl H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 59.84 5.32 Found 59.40 5.21 199 CH.sub.3 H H Cl H Cl H H H CH.sub.3 H H C H A A Calc. 57.71 4.20 Found 57.74 4.47 200 (CH.sub.2).sub.4 CH.sub.3 H H Cl H Cl H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 63.48 6.60 Found 63.69 6.63 201 (CH.sub.2).sub.4 CH.sub.3 H H Cl H Cl H H H CH.sub.3 H H C H A A Calc. 61.81 6.00 Found 62.20 6.09 202 ##STR91## CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H 119-120 B A 203 ##STR92## CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H Calc.Found 7 C8.3578.36 H 9.86 9.35 A A 204 ##STR93## CH.sub.3 H CH.sub.3 H CH.sub.3 H H H C.sub.2 H.sub.5 H H Calc.Found C78.0878.42 H 9.44 9.14 A A 205 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H H H H 83-84 A A 206 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H ##STR94## H H Calc.Found C77.9377.05 H 8.53 8.52 A A 207 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 76.40 8.33 Found 76.37 8.36 208 CH.sub.3 CH.sub. 3 H CH.sub.3 H CH.sub.3 H H H CH.sub.3 H H C H A A Calc. 75.50 7.74 Found 75.21 7.80 209 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H C.sub.2 H.sub.5 H H C H A A Calc. 75.97 8.05 Found 76.04 8.09 210 C.sub.2 H.sub.5 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H C(CH.sub.3).sub.3 H H 69.5-72.5 A A 211 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H C(CH.sub.3).sub.3 H H C H A A Calc. 78.08 9.44 Found 78.65 9.63 212 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.80 9.25 Found 76.81 9.42 213 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H CH.sub.3 H H C H A A Calc. 76.33 9.15 Found 77.04 8.99 214 (CH.sub.2).sub.4 CH.sub.3 CH.sub.3 H CH.sub.3 H CH.sub.3 H H H C.sub.2 H.sub.5 H H C H A A Calc. 77.49 9.05 Found 77.76 9.20 215 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 75.97 8.05 Found 73.58 7.52 216 C.sub.2 H.sub.5 H H CH.sub.3 H CH.sub.3 H H H C(CH.sub.3).sub.2 H H C H A A Calc. 76.80 8.59 Found 75.86 8.52 217 C.sub.2 H.sub.5 H H CH.sub.3 H CH.sub.3 H H H CH(C.sub.2 H.sub.5).sub.2 H H C H A A Calc. 77.15 8.83 Found 77.34 8.92 218 (CH.sub.2).sub.4 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H C(CH.sub.3).sub.3 H H C H A A Calc. 77.80 9.25 Found 78.18 9.28 219 (CH.sub.2).sub.4 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H C H A A Calc. 77.49 9.05 Found 77.20 9.14 220 (CH.sub.2).sub.4 CH.sub.3 H H CH.sub.3 H CH.sub.3 H H H CH(C.sub.2 H.sub.5).sub.2 H H C H A A Calc. 78.08 9.44 Found 78.07 9.64 221 ##STR95## H H H H CH.sub.3 H H H CH(CH.sub.3).sub.2 H H Calc.Found C77.7977.95 H 9.25 8.99 A A 222 ##STR96## H H H H CH.sub.3 H H CH.sub.3 (CH.sub.2).sub.4 CH.sub.3 H H Calc.Found 7 C8.5979.17 H 9.77 9.98 A C 223 CH.sub.3 H H H H CH.sub.3 H H H C.sub.2 H.sub.5 H H C H A A Calc. 74.97 7.40 Found 75.10 7.28 224 CH.sub.3 H H H H CH.sub.3 H H H CH.sub.3 (CH.sub.2).sub.2 H H C H A A Calc. 75.50 7.74 Found 75.47 7.42 225 CH.sub.3 H H H H CH.sub.3 H H CH.sub.3 (CH.sub.2).sub. 4 CH.sub.3 H H C H A A Calc. 76.79 8.59 Found 76.14 8.32 226 CHC(CH.sub.3).sub.2 H H H H CH.sub.3 H H CH.sub.3 CH.sub.3 H H 57-58 A A 227 (CH.sub.2).sub.14 CH.sub.3 H H H H CH.sub.3 H H CH.sub.3 (CH.sub.2).sub.4 CH.sub.3 H H C H B C Calc. 80.10 10.76 Found 80.42 10.43 228 (CH.sub.2).sub.4 CH.sub.3 H H H H CH.sub.3 H H H C.sub.2 H.sub.5 H H C H A A Calc. 76.79 8.59 Found 76.85 8.54 229 (CH.sub.2).sub.4 CH.sub.3 H H H H CH.sub.3 H H H CH.sub.3 (CH.sub.2).sub.2 H H C H A A Calc. 77.16 8.83 Found 76.19 8.98 230 (CH.sub.2).sub.4 CH.sub.3 H H H H CH.sub.3 H H CH.sub.3 (CH.sub.2).sub.4 CH.sub.3 H H C H A A Calc. 78.08 9.44 Found 78.54 9.56

It will be understood that the plant species employed in the above tests are merely representative of a wide variety of plant pest that can be controlled by the use of the compounds of this invention. The compounds contemplated in this invention may be applied as mite ovicides, miticides and pre-emergent herbicides according to methods known to those skilled in the art. Pesticidal compositions containing the compounds as the active toxicant will usually comprise a carrier and/or diluent, either liquid or solid.

Suitable liquid diluents or carriers include water, petroleum distillates, or other liquid carriers with or without surface active agents. Liquid concentrates may be prepared by dissolving one of these compounds with a nonphytotoxic solvent such as acetone, xylene, or nitrobenzene and dispersing the toxicants in water with the aid of suitable surface active emulsifying and dispersing agents.

The choice of dispersing and emulsifying agents and the amount employed is dictated by the nature of the composition and the ability of the agent to facilitate the dispersion of the toxicant. Generally, it is desirable to use as little of the agent as is possible, consistent with the desired dispersion of the toxicant in the spray so that rain does not re-emulsify the toxicant after it is applied to the plant and wash it off the plant. Nonionic, anionic, amphoteric or cationic dispersing an emulsifying agents may be employed, for example, the condensation products of alkylene oxides with phenol and organic acids, alkyl aryl sulfonates, complex ether alcohols, quaternary ammonium compounds, and the like.

In the preparation of wettable powder or dust or granulated compositions, the active ingredient is dispersed in and on an appropriately divided solid carrier such as clay, talc, bentonite, diatomaceous earth, fullers earth, and the like. In the formulation of the wettable powders the aforementioned dispersion agents as well as lignosulfonates can be included.

The required amount of the toxicants contemplated herein may be applied per acre treated in from 1 to 200 gallons or more of liquid carrier and/or diluent or in from about 5 to 500 pounds of inert solid carrier and/or diluent. The concentration in the liquid concentrate with usually vary from about 10 to 95 percent by weight and in the solid formulations from about 0.5 to about 90 percent by weight. Satisfactory sprays, dusts, or granules for general use contain from about 1/4 to 15 pounds of active toxicant per acre.

The pesticides contemplated herein prevent attack by insects and mites upon plants or other material to which the pesticides are applied, and they have relatively high residual toxicity. With respect to plants, they have a high margin of safety in that when used in sufficient amount to kill or repel the insects, they do not burn or injure the plant, and they resist weathering which includes wash-off caused by rain, decomposition by ultra violet light, oxidation, or hydrolysis in the presence of moisture or, at least such decomposition, oxidation, and hydrolysis as would materially decrease the desirable pesticidal characteristic of the toxicants or impart undesirable characteristics, for instance, phytotoxicity, to the toxicants. The toxicants are so chemically inert that they are compatible with substantially any other constituents of the spray schedule, and they will be used in the soil, upon the seeds, or the roots of plants without injuring either the seeds or roots of plants. They may also be used in combination with other pesticidally active compounds. When used as miticides they will normally be applied to the foliage of the plants to be treated. When used as herbicides they may be used in the soil or directly upon the seeds to be treated. The compounds of this invention may also be used in combination with other pesticidally active materials.