N-(Phenylcycloalkyl)acetamide derivatives, and their production and use

Abstract

A compound of the formula: ##STR1## wherein R.sub.1 and R.sub.2, which may be the same or different, are each a C.sub.1 -C.sub.3 alkyl group, a chloromethyl group or a halogen atom, R.sub.3 is a hydrogen atom, a methyl group or a halogen atom, n is an integer of 2 to 5 and X is a hydrogen atom, a methyl group, a methoxy group or a chlorine atom, which is useful as a herbicide.

Description

The present invention relates to N-(phenylcycloalkyl)acetamide derivatives, and their production and use. More particularly, it relates to N-(phenylcycloalkyl)acetamide derivatives and herbicidal compositions comprising them, and to preparation processes therefor.

The said N-(phenylcycloalkyl)acetamide derivatives are representable by the formula: ##STR2## wherein R.sub.1 and R.sub.2, which may be the same or different, are each a C.sub.1 -C.sub.3 alkyl group, a chloromethyl group or a halogen atom, R.sub.3 is a hydrogen atom, a methyl group or a halogen atom, n is an integer of 2 to 5 and X is a hydrogen atom, a methyl group, a methoxy group or a chlorine atom.

The term "halogen atom" as hereinabove used is intended to mean chlorine, bromine, fluorine and iodine, inclusively.

As the result of an extensive study, it has been found that the N-(phenylcycloalkyl)acetamide derivatives (I) have a strong herbicidal activity against a wide variety of weeds. For instance, they can exert a notable controlling or eradicating activity on the following annual and perennial weeds by pre-emergence soil treatment or post-emergence foliar or soil treatments: Gramineae weeds such as barnyard-grass (Echinochloa crus-galli), large crabgrass (Digitaria sanguinalis), green foxtail (Setaria viridis), Johnsongrass (Sorghum halepense) and bermudagrass (Cynodon dactylon), Cyperaceae weeds such as yellow nutsedge (Cyperus esculentus), nutsedge sp. (Cyperus difformis), purple nutsedge (Cyperus rotundus), Scirpus Hotarui, slender spikebrush (Eleocharis acicularis), Cyperus serotinus and Eleocharis kuroguwai, Amaranthaceae weeds such as redroot pigweed (Amarantus retroflexus), Chenopodiaceae weeds such as common lambsquarters (Chenopodiu album), Polygonaceae such as ladysthumb (Polygonum persicaria) and curlydock (Rumex japonicus), Pontederiaceae such as Monochoria vaginalis, Scrophulariaceae such as false pimpernel (Lindernia pyxidaria), Alismataceae such as arrowhead (Sagittaria pygmaea), Compositae such as dandelion (Taraxacum officinale), Oxalidaceae such as woodsorrel (Oxalis corniculata), etc. Thus, their herbicidal activity is effective in controlling and eradicating not only field weeds but also paddy field weeds.

Advantageously, the N-(phenylcycloalkyl)acetamide derivatives (I) do not produce any injury on various crop plants such as rice, soybean, cotton, peanut, sunflower, rape and potato and numerous vegetables such as cabbage, tomato and carrot.

Accordingly, the N-(phenylcycloalkyl)acetamide derivatives (I) are useful as herbicides applicable for field crops and vegetables as well as paddy rice. They are also useful as herbicides to be employed for orchard, lawn, pasture, tea garden, mulberry field, rubber plantation, forest, etc. utilities.

Japanese Patent Publication (unexamined) No. 88228/1973 and U.S. Pat. No. 3,498,781 disclose some pivalic acid amide derivatives, which are somewhat similar to the N-(phenylcycloalkyl)acetamide derivatives (I) in chemical structure and have a herbicidal activity. However, the herbicidal activity of the N-(phenylcycloalkyl)acetamide derivatives (I) is generally more excellent than that of the pivalic acid amide herbicidals. It is particularly notable that, in comparison with the pivalic acid amide derivatives, the N-(phenylcycloalkyl)acetamide derivatives (I) exert an extremely high herbicidal effect on annual and perennial weeds in paddy fields without any phytotoxicity on rice plants. Further, the N-(phenylcycloalkyl)acetamide derivatives (I) are quite characteristic in being highly effective for selectively controlling or eradicating Gramineae weeds and perennial Cyperaceae weeds in the cultivation of the crop plant and the vegetables.

The N-(phenylcycloalkyl)acetamide derivatives (I) can be produced by reacting a substituted acetic acid of theformula: ##STR3## wherein R.sub.1, R.sub.2 and R.sub.3 are each as defined above, or its reactive derivative with a phenylcycloalkylamine compound of the formula: ##STR4## wherein n and X are each as defined above.

The substituted acetic acid (II) may be synthesized, for instance, by the method as disclosed in J. Chem. Soc., Perkin I, 694 (1977). The phenylcycloalkylamine compound (III) is obtainable, for instance, by the method as disclosed in Israel J. Chem., 5, 223 (1967).

For the reaction, the substituted acetic acid (II) or is reactive derivative and the phenylcycloalkylamine compound (III) may be used in an equivalent ratio of 0.4 to 1.5:1, preferably 0.5 to 1.1:1. The reaction may be carried out in the presence or absence of an inert solvent. Examples of the inert solvent are hydrocarbons (e.g. benzene, toluene, xylene), halogenated hydrocarbons (e.g. chlorobenzene, methylene chloride, chloroform, carbon tetrachloride), ethers (e.g. diisopropyl ether, tetrahydrofuran, dioxane), alcohols (e.g. methanol, ethanol, isopropanol), ketones (e.g. acetone, methylethylketone, methylisobutylketone), esters (e.g. ethyl acetate), nitriles (e.g. acetonitrile), dimethylsulfoxide, dimethylformamide, water, etc. Among them, particularly preferred is benzene. The reaction may be carried out within a wide range of temperature from the freezing point to the boiling point of the solvent, preferably from 0.degree. C. to the boiling temperature of the solvent. If necessary, cooling or heating may be adopted.

As the substituted acetic acid (II) or its reactive derivative, there may be used the free acid, acid anhydride, acid chloride, acid bromide, acid ester, etc. Depending upon the kind of the reactive derivative, an appropriate reaction aid such as a condensing agent, a dehydrating agent, an acid-eliminating agent or a catalyst may be employed in the reaction. In the case of the free acid, dicyclohexylcarbodiimide, phosphorus pentachloride, phosphorus trichloride, phosphorus tribromide, thionyl chloride, sodium hydroxide, potassium hydroxide, sodium methoxide, sodium ethoxide, triethylamine, pyridine, quinoline, isoquinoline, N,N-dimethylaniline, N,N-diethylaniline, N-methylmorpholine, etc. are examples of the reaction aid. In case of the acid chloride or acid bromide, sodium hydroxide, potassium hydroxide, sodium methoxide, sodium ethoxide, triethylamine, pyridine, quinoline, isoquinoline, N,N-dimethylaniline, N,N-diethylaniline, N-methylmorpholine, sodium acetate, etc., preferably triethylamine, are usable as the reaction aid. When the reaction aid is employed, its amount may be from a catalytic amount to 1.5 equivalents, preferably from 0.95 to 1.1 equivalents with respect to the material to be eliminated from the starting compounds as the result of the reaction.

The recovery of the reaction product from the reaction mixture may be carried out in a per se conventional manner. For instance, the reaction mixture is filtered and/or washed with water, followed by distillation for removal of the solvent to give the reaction product, i.e. the N-(phenylcycloalkyl)acetamide derivative (I). When desired, this reaction product may be purified by a per se conventional procedure such as recrystallization from an appropriate solvent such as benzene, toluene, n-hexane, methanol, ethanol, chloroform or methylisobutylketone.

Practical embodiments of the preparation of the N-(phenylcycloalkyl)acetamide derivatives (I) are illustratively shown in the following examples.

EXAMPLE 1

(1) Into a 200 ml four-necked flask, there were charged benzene (100 ml), 1-phenylcycloalkylamine (8.1 g) and triethylamine (6.1 g), and trimethylacetyl chloride (6.0 g) was dropwise added thereto while stirring at room temperature. Stirring was continued for 3 hours. After completion of the reaction, the reaction mixture was washed with water to remove triethylamine hydrochloride. After the benzene layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was recrystallized from ethanol to give 10.6 g of N-(1-phenylcyclopentyl)trimethylacetamide. M.P., 142.degree.-143.degree. C.

Elementary analysis: Calcd.: C, 78.32%; H, 9.45%; N, 5.71%. Found: C, 78.44%; H, 9.36%; N, 5.62%.

(2) Into a 500 ml four-necked flask, there were charged methylisobutylketone (150 ml), 1-phenylcyclopentylamine (24.3 g) and triethylamine (16.0 g), and trimethylacetyl chloride (18.0 g) was dropwise added thereto while stirring at room temperature. Stirring was continued for 3 hours. After completion of the reaction, water (200 ml) was added thereto and the reaction mixture was gradually heated to remove methylisobutylketone, followed by cooling at room temperature. The precipitated crystals were filtered, washed with water, dried and recrystallized from ethanol to give N-(1-phenylcyclopentyl)trimethylacetamide (33.4 g).

EXAMPLE 2

Into a 200 ml four-necked flask, there were charged benzene (100 ml), 1-(p-methylphenyl)cyclopentylamine (8.8 g) and triethylamine (6.1 g), and trimethylacetyl chloride (6.0 g) was dropwise added thereto while stirring at room temperature. Stirring was continued for 3 hours. After completion of the reaction, the reaction mixture was washed with water to remove triethylamine hydrochloride. After the benzene layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was recrystallized from ethanol to give 10.8 g of N-[1-(p-methylphenyl)cyclopentyl]trimethylacetamide. M.P., 166.degree.-167.degree. C.

Elementary analysis: Calcd.: C, 78.72%; H, 9.71%; N, 5.40%. Found: C, 78.99%; H, 9.50%; N, 5.46%.

EXAMPLE 3

Into a 200 ml four-necked flask, there were charged toluene (150 ml), 1-phenylcyclohexylamine (10.5 g) and pyridine (5.2 g), and trimethylacetyl chloride (7.2 g) was dropwise added thereto while stirring at room temperature. Stirring was continued for 3 hours. After completion of the reaction, the reaction mixture was washed with water to remove pyridine hydrochloride. The toluene layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was recrystallized from ethanol to give 9.8 g of N-(1-phenylcyclohexyl)trimethylacetamide. M.P., 129.degree.-130.5.degree. C.

Elementary analysis: Calcd.: C, 78.72%; H, 9.71%; N. 5.40%. Found: C, 78.91%; H, 9.69%; N, 5.34%.

EXAMPLE 4

Into a 200 ml four-necked flask, there were charged benzene (100 ml), 1-phenylcyclopentylamine (8.1 g) and triethylamine (6.1 g), and trichloroacetyl chloride (9.1 g) was dropwise added thereto while stirring at room temperature. Stirring was continued for 3 hours. After completion of the reaction, the reaction mixture was washed with water to remove triethylamine hydrochloride. The benzene layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was recrystallized from ethanol to give 12.4 g g of N-(1-phenylcyclopentyl)trichloroacetamide. M.P., 114.degree.-115.5.degree. C.

Elementary analysis: Calcd.: C, 50.92%; H, 4.60%; N, 4.57%; Cl, 34.69%. Found: C, 50.95%; H, 4.61%; N, 4.70%; Cl, 34.53%.

In the same manner as above, there can be produced other N-(phenylcycloalkyl)acetamicde derivatives (I), of which some specific examples will be shown in Table 1 but without any intention to limit the scope of the invention thereto:

TABLE 1__________________________________________________________________________ ##STR5##Com. Meltingpound point Elementary analysis (%)No. R.sub.1 R.sub.2 R.sub.3 N X (.degree.C.) C H N Halogen__________________________________________________________________________1 C.sub.2 H.sub.5 CH.sub.3 H 4 H 135.5- Calcd. 78.32 9.45 5.71 136.5 Found 78.49 9.69 5.742 C.sub.2 H.sub.5 C.sub.2 H.sub.5 H 4 H 163- Calcd. 78.72 9.71 5.40 165.5 Found 78.74 9.85 5.273 i-C.sub.3 H.sub.7 CH.sub.3 H 4 H 157- Calcd. 78.72 9.71 5.40 158 Found 78.88 9.85 5.194 i-C.sub.3 H.sub.7 i-C.sub.3 H.sub.7 H 4 H 173- Calcd. 79.39 10.17 4.87 174.5 Found 79.50 10.22 4.655 CH.sub.3 CH.sub.3 CH.sub.3 2 H 112- Calcd. 77.38 8.81 6.45 114 Found 77.25 8.90 6.336 CH.sub.3 CH.sub.3 CH.sub.3 2 4-Cl 109- Calcd. 66.79 7.21 5.56 14.08 (Cl) 110 Found 66.90 7.31 5.63 14.19 (Cl)7 CH.sub.3 CH.sub.3 CH.sub.3 3 H 154.5- Calcd. 77.88 9.15 6.05 156 Found 77.87 9.26 5.908 CH.sub.3 CH.sub.3 CH.sub.3 3 4-Cl 142- Calcd. 67.79 7.58 5.27 13.34 (Cl) 143 Found 67.84 7.72 5.39 13.47 (Cl)9 CH.sub.3 CH.sub.3 CH.sub.3 4 H 142- Calcd. 78.32 9.45 5.71 143 Found 78.44 9.36 5.6210 CH.sub.3 CH.sub.3 CH.sub.3 4 2-CH.sub.3 126- Calcd. 78.72 9.71 5.40 127.5 Found 78.68 9.88 5.3511 CH.sub.3 CH.sub.3 CH.sub.3 4 3-CH.sub.3 115- Calcd. 78.72 9.71 5.40 117 Found 78.70 9.78 5.4512 CH.sub.3 CH.sub.3 CH.sub.3 4 4-CH.sub.3 166- Calcd. 78.72 9.71 5.40 167 Found 78.99 9.50 5.4613 CH.sub.3 CH.sub.3 CH.sub.3 4 4-Cl 140.5- Calcd. 68.68 7.92 5.01 12.67 (Cl) 141.5 Found 68.80 8.11 5.19 12.52 (Cl)14 CH.sub.3 CH.sub.3 CH.sub.3 4 4-OCH.sub.3 134- Calcd. 74.14 9.15 5.09 135 Found 74.23 9.28 5.0915 CH.sub.3 CH.sub.3 CH.sub.3 5 H 129- Calcd. 78.72 9.71 5.40 130.5 Found 78.91 9.69 5.3416 C.sub.2 H.sub.5 CH.sub.3 CH.sub.3 4 H 129.5- Calcd. 78.72 9.71 5.40 131 Found 78.80 9.68 5.4317 n-C.sub.3 H.sub.7 CH.sub.3 CH.sub.3 4 H 137- Calcd. 79.07 9.95 5.12 139 Found 79.10 9.87 5.2018 i-C.sub.3 H.sub.7 CH.sub.3 CH.sub.3 4 H 135- Calcd. 79.07 9.95 5.12 136.5 Found 78.86 9.75 5.2319 i-C.sub.3 H.sub.7 i-C.sub.3 H.sub.7 CH.sub.3 4 H 75.5- Calcd. 79.68 10.36 4.65 76.5 Found 79.83 10.52 4.3920 ClCH.sub.2 CH.sub.3 CH.sub.3 4 H 127- Calcd. 68.68 7.92 5.01 12.67 (Cl) 128.5 Found 68.51 8.17 5.24 12.77 (Cl)21 ClCH.sub.2 ClCH.sub.2 CH.sub.3 4 H 125- Calcd. 61.15 6.74 4.46 22.56 (Cl) 126 Found 61.02 6.81 4.38 22.67 (Cl)22 Br CH.sub.3 CH.sub.3 4 H 93-95 Calcd. 58.07 6.50 4.51 25.76 (Br) Found 58.12 6.62 4.69 25.58 (Br)23 F F F 4 H 99-101 Calcd. 60.70 5.49 5.44 Found 60.81 5.38 5.2924 Cl Cl Cl 4 H 114- Calcd. 50.92 4.60 4.57 34.69 (Cl) 115.5 Found 50.95 4.61 4.70 34.53 (Cl)25 Br Br Br 4 H 108- Calcd. 35.49 3.21 3.18 54.48 (Br) 111 Found 35.22 3.15 2.97 54.73 (Br)__________________________________________________________________________

In the practical usage of the N-(phenylcycloalkyl)acetamide derivatives (I), they may be applied as such or in preparation form such as granules, fine granules, dusts, coarse dusts, wettable powders, emulsifiable concentrates, flowable formulations, aqueous concentrates or oily suspensions.

In producing such preparation forms, solid or liquid carrriers may be used. As for the solid carrier, there may be mentioned mineral powders (e.g. kaolin, bentonite, clay, montmorillonite, talc, diatomaceous earth, mica, vermiculite, gypsum, calcium carbonate, apatite), vegetable powders (e.g. soybean powder, flour, wooden powder, tobacco powder, starch, crystalline cellulose), high molecular weight compounds (e.g. petroleum resin, polyvinyl chloride, dammar gum, ketone resin), alumina, wax and the like.

As for the liquid carrier, there may be mentioned kerosene, alcohols (e.g. methanol, ethanol, ethylene glycol, benzyl alcohol), aromatic hydrocarbons (e.g. toluene, benzene, xylene, methylnaphthalene), halogenated hydrocarbons (e.g. chloroform, carbon tetrachloride, monochlorobenzene), ethers (e.g. dioxane, tetrahydrofuran), ketones (e.g. acetone, methylethylketone, cyclohexanone, isophorone), esters (e.g. ethyl acetate, buty acetate, ethylene glycol acetate), acid amides (e.g. dimethylformamide), nitriles (e.g. acetonitrile), ether alcohols (e.g. ethylene glycol ethyl ether), water and the like.

A surface active agent used for emulsification, dispersion or spreading may be any of the non-ionic, anionic, cationic and amphoteric type of agents. Examples of the surface active agent include polyoxyethylene alkyl ethers, polyoxyethylene alkylaryl ethers, polyoxyethylene fatty acid esters, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters, oxyethylene-oxypropylene polymers, polyoxyethylene alkyl phosphates, fatty acid salts, alkyl sulfates, alkyl sulfonates, alkylaryl sulfonates, alkyl phosphtes, polyoxyethylene alkyl sulfates, quaternary ammonium salts and the like. But, the surface active agent is not of course limited to these compounds. And, if necessary, gelatin, casein, sodium alginate, starch, agar, polyvinyl alcohol or the like may be used as an auxiliary agent.

In the preparation of a herbicidal composition, the content of the N-(phenylcycloalkyl)acetamide derivative (I) may be usually from 0.05 to 95% by weight, preferably from 3 to 50% by weight.

Practical embodiments of the herbicidal compositions according to the invention are illustratively shown in the following examples wherein parts and % are by weight.

PREPARATION EXAMPLE 1

Fifty parts of Compound No. 2, 2.5 parts of a dodecylbenzenesulfonate, 2.5 parts of a ligninsulfonate and 45 parts of diatomaceous earth are well mixed while being powdered to obtain a wettable powder.

PREPARATION EXAMPLE 2

Thirty parts of Compound No. 3, 10 parts of emulsifier ("Sorpol SM-100" manufactured by Toho Chemical Co., Ltd.) and 60 parts of xylene are well mixed to obtain an emulsifiable concentrate.

PREPARATION EXAMPLE 3

Five parts of Compound No. 9, 1 part of white carbon, 5 parts of a ligninsulfonate and 89 parts of clay are well mixed while being powdered. The mixture is then well kneaded with water, granulated and dried to obtain a granule.

PREPARATION EXAMPLE 4

Thirty parts of Compound No. 12, 1 part of isopropyl phosphate, 66 parts of clay and 30 parts of talc are well mixed while being powdered. The mixture is then kneaded with water, granulated and dried to obtain a granule.

PREPARATION EXAMPLE 5

Forty parts of bentonite, 5 parts of a lignin-sulfonate and 55 parts of clay are well mixed while being powdered. The mixture is then well kneaded with water, granulated and dried to obtain a granule containing no active ingredient. The granule is then impregnated with 5 parts of Compound No. 15 dissolved in acetone. Subsequent removal of acetone gives a granule.

PREPARATION EXAMPLE 6

Ninety-seven parts of bentonite of 16-48 mesh is impregnated with 3 parts of Compound No. 20 dissolved in acetone. Subsequent removal of acetone gives a granule.

The N-(phenylcycloalkyl)acetamide derivative (I) may be used together with other herbicides to improve their activity as herbicides, and in some cases, a synergistic effect may be expected. As the herbicides to be mixed therewith, there may be exemplifid phenoxy series herbicides such as 2,4-dichlorophenoxyacetic acid, 2-methyl-4-chlorophenoxyacetic acid and 2-methyl-4-chlorophenoxybutyric acid (including esters and salts thereof); benzoic acid series herbicides such as 3,6-dichloro-2-methoxybenzoic acid and 2,5-dichloro-3-aminobenzoic acid; diphenyl ether series herbicides such as 2,4-dichlorophenyl-4'-nitrophenyl ether, 2,4,6-trichlorophenyl-4'-nitrophenyl ether, 2-chloro-4-trifluoromethylphenyl-3'-ethoxy-4'-nitrophenyl ether, 2,4-dichlorophenyl-4'-nitro-3'-methoxyphenyl ether, 2,4-dichlorophenyl-3'-methoxycarbonyl-4'-nitrophenyl ether and sodium 5-(2'-chloro-4'-trifluoromethylphenoxy)-2-nitrobenzoate; triazine series herbicides such as 2-chloro-4,6-bisethylamino-1,3,5-triazine, 2-chloro-4-ethylamino-6-isopropylamino-1,3,5-triazine, 2-methylthio-4,6-bisethylamino-1,3,5-triazine, 2-methylthio-4,6-bisisopropylamino-1,3,5-triazine and 4-amino-6-tert-butyl-3-methylthio-1,2,4-triazin-5-one; urea series herbicides such as 3-(3,4-dichlorophenyl)-1,1-dimethylurea, 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea, 1-(2,2-dimethylbenzyl)-3-p-tolylurea and 1-(2,2-dimethylbenzyl)-3-methyl-3-phenylurea; carbamate series herbicides such as isopropyl-N-(3-chlorophenyl)carbamate and methyl-N-(3,4-dichlorophenyl)carbamate; thiolcarbamate series herbicides such as S-ethyl-N,N-dipropylthiolcarbamate, S-(4-chlorobenzyl)-N,N-diethylthiolcarbamate, S-ethyl-N,N-hexamethylene-thiolcarbamate, S-2,3-dichloroallyl-N,N-diisopropylthiol-carbamate and S-ethyl-N,N-dibutylthiolcarbamate; acid anilide series herbicides such 3,4-dichloropropionanilide, N-methoxymethyl-2,6-diethyl-60-chloroacetanilide, 2-chloro-2',6'-diethyl-N-butoxymethylacetanilide, 2-chloro-2',6'-diethyl-N-(n-propoxyethyl)acetanilide and N-chloroacetyl-N-(2,6-diethyophenyl)glycineethyl ester; uracil series herbicides such as 5-bromo-3-sec-butyl-6-methyluracil and 3-cyclohexyl-5,6-trimethyleneuracil; pyridinium chloride series herbicides such as 1,1'-dimethyl-4,4-bispyridinium chloride, phosphorus series herbicides such as N-(phosphonomethyl)glycine, O-ethyl-O-(2-nitro-5-methylphenyl)-N-sec-butylphosphoramidothioate, S-(2-methyl-1-piperidylcarbonylmethyl) O,O-di-n-propyldithiophosphate and S-(2-methyl-1-piperidylcarbonylmethyl) O,O-diphenyldithiophosphate; toluidine series herbicides such as .alpha.,.alpha.,.alpha.-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine; aliphatic compounds series herbicides such trichloroacetic acid, 2,2-dichloropropionic acid and 2,2,3,3-tetrafluoropropionic acid; 5-tert-butyl-3-(2,4-dichloro-5-isopropoxyphenyl)-1,3,4-oxadiazolin-2-one; 3-isopropyl-1H-2,1,3-benzothiadiazin(4)-3H-one-2,2-dioxide; 2,6-dichlorobenzonitrile; .alpha.-(.beta.-naphthoxy)propionanilide; 4'-(phenylsulfonyl)-(1,1,1-trifluoromethylsulphono)-O-toluidide; 4-(2,4-dichlorobenzyl)-1,3-dimethylpyrazole-5-yl-p-toluene-sulfonate; N-p-chlorobenzyloxyphenyl)-.DELTA.'-tetrahydrophthalimide and the like. But, the herbicides are not of course limited to these examples.

The herbicides of the invention may be applied together with fungicides, pyrethroid series insecticides, other insecticides, plant growth regulators, fertilizers, etc.

When the N-(phenylcycloalkyl)acetamide derivative (I) is used as a herbicide, it may be applied before or after germination of weeds in an amount within a wide range. The amount may be usually from about 0.1 to 1 kilogram per hectare, preferably from about 0.25 to 5 kilograms per hectare.

Some test samples which show the herbicidal activity of the N-(phenylcycloalkyl)acetamide derivatives (I) are shown in the following Examples wherein % is by weight.

EXAMPLE I

A Wagner's pot of 14 cm in diameter was filled with 1.5 kg of paddy field soil and water was added thereto to simulate paddy field conditions. Rice seedlings of the 3-leaf growth stage were transplanted in the pot, and seeds of barnyard grass (Echinochloa cruss-galli) and Scirpus Hotarui, and buds of slender spikerush (Eleocharis aciculalis), which tided over the winter, were further sowed therein. A required amount of each test compound was applied to the soil under water-lodged condition. Twenty-five days after the application, the herbicidal activity and phytotoxicity of the test compound were checked on the transplanted and sowed plants and spontaneously germinated Monochoria vaginalis. The results are shown in Table 2.

As to the application, a wettable powder containing a required amount of the test compound was diluted with water and applied in a proportion of 10 ml/pot by means of a pipette. The herbicidal activity was evaluated in figures ranging from 0 to 5.

______________________________________Figures Percentage of inhibition (%)______________________________________0 0- 91 10-292 30-493 50-694 70-895 90-100______________________________________

As to the evaluation of phytotoxicity, the three factors (i.e. height of plant, number of tillers and total weight (dry weight)) were each checked, and a ratio of the treated plot to the untreated plot was calculated for each factor. The phytotoxicity was evaluated based on the lowest value of the three ratios which was classified into the following grades ranging from 0 to 5.

______________________________________Grade Ratio of the untreated plot (%)______________________________________0 1001 90-992 80-893 60-794 40-595 0-39______________________________________ TABLE 2______________________________________Dosage(weightof Herbicidal activity Phyto- active Mono- Scir- Slender toxi-Com- ingre- Barn- choria- pus spi- citypound dient yard vagin- Hota- ker RiceNo. g/are) grass alis rui rush plant______________________________________ 1 40 5 4 5 5 0 20 4 4 4 5 0 2 40 5 5 5 5 0 20 5 5 5 5 0 3 40 -- 5 5 5 0 20 -- 4 4 5 0 4 40 -- 5 5 5 0 20 -- 5 4 5 0 5 40 5 5 5 5 0 20 5 4 5 5 0 6 40 5 5 5 5 0 20 4 4 4 5 0 7 40 5 5 5 5 0 20 4 5 5 5 0 8 40 -- 5 5 5 0 20 -- 4 5 5 0 9 40 5 5 5 5 0 20 5 5 5 5 010 40 -- 4 5 5 0 20 -- 4 4 5 011 40 -- 5 4 5 0 20 -- 4 5 5 012 40 5 5 5 5 0 20 5 5 5 5 013 40 5 5 4 5 0 20 5 4 4 4 014 40 -- 4 5 5 0 20 -- 4 4 4 015 40 5 5 5 5 0 20 5 5 5 5 016 40 -- 5 5 4 0 20 -- 4 5 4 017 40 -- 5 5 5 0 20 -- 4 5 4 018 40 -- 4 5 5 0 20 -- 4 5 4 019 40 -- 4 4 5 0 20 -- 4 4 5 020 40 5 5 5 5 0 20 5 4 5 5 021 40 5 5 4 5 0 20 4 4 4 5 022 40 5 5 5 5 0 20 4 4 5 5 023 40 4 5 5 5 0 20 4 4 5 5 024 40 5 5 5 5 0 20 4 5 4 5 024 40 5 5 5 5 0 20 4 5 4 5 025 40 5 4 5 5 0 20 4 4 5 5 0Un- -- 0 0 0 0 0treat-ed______________________________________

EXAMPLE II

The seeds of weeds such as large crabgrass (Digitaria sanguinalis), redroot pigweed (Amaranthus retroflexus), green foxtail (Setaria viridis), tubers of purple nutsedge (Cyperus rotundus) and seeds of crops such as peanut and cotton were each sowed in a 10 cm flower pot and covered with soil. Separately, a required amount of each test compound was formulated into an emulsifiable concentrate and diluted with water. The diluted chemical solution was applied to the soil by means of a hand sprayer and the thus treated soil was mixed and kept to the depth of 2 cm from the soil surface. Each of the weeds and crops was grown up in a green-house, and the herbicidal activity and phytotoxicity of the test compound were checked 20 days after the application. The test results are shown in Table 3. The herbicidal activity was evaluated in figures ranging from 0 to 5. The phytotoxicity to the crop plants was also indicated on the same standard as that of the herbicidal activity.

______________________________________Figures Percentage of inhibition (%)______________________________________0 0- 91 10-292 30-493 50-694 70-895 90-100______________________________________ TABLE 3______________________________________Dosage(weight Herbicidal activity of ac- Red- Phyto-Com- tive in- Purple Large root Green toxicitypound gredient, nut- crab- pig- fox- Pea- Cot-No. a/are) sedge grass weed tail nut ton______________________________________1 80 5 5 5 5 0 0 40 4 5 4 5 0 02 80 5 5 5 5 0 0 40 5 5 5 5 0 05 80 5 5 5 5 0 0 40 4 5 5 5 0 06 80 5 5 5 5 0 0 40 4 5 5 5 0 07 80 5 5 5 5 0 0 40 4 5 4 5 0 08 80 5 5 5 5 0 0 40 5 5 4 5 0 09 80 5 5 5 5 0 0 40 5 5 5 5 0 012 80 5 5 5 5 0 0 40 5 5 5 5 0 013 80 4 5 4 5 0 0 40 3 5 4 5 0 015 80 5 5 5 5 0 0 40 5 5 5 5 0 016 80 5 5 5 5 0 0 40 5 5 5 5 0 020 80 5 5 5 5 0 0 40 5 5 4 5 0 022 80 5 5 5 5 0 0 40 5 5 4 5 0 0A*.sup.1 80 0 0 1 0 0 0 40 0 0 0 0 0 0B*.sup.2 80 0 3 3 3 3 2 40 0 2 1 1 2 1C*.sup.3 80 0 1 1 0 0 0 40 0 0 0 0 0 0D*.sup.4 80 0 0 0 0 0 0 40 0 0 0 0 0 0______________________________________ Note: *.sup.1 Compound disclosed in Japanese Patent Publication (unexamined) No 88228/1973: ##STR6## *.sup.2 Compound disclosed in U.S. Pat. No. 3,498,781:? ##STR7## *.sup.3 Compound disclosed in Israel J.Chem., 5, 223 (1967): ##STR8## *.sup.4 Compound disclosed in Israel J. Chem., 5, 223 (1967) ##STR9##

Claims

1. A compound of the formula: ##STR10## wherein R.sub.1 and R.sub.2, which may be the same or different, are each a C.sub.1 -C.sub.3 alkyl group, a chloromethyl group or a halogen atom, R.sub.3 is a hydrogen atom, a methyl group or a halogen atom, n is an integer of 2 to 5 and X is a hydrogen atom, a methyl group, a methoxy group or a chlorine atom.

2. The compound according to claim 1, wherein R.sub.1 is a methyl group or an ethyl group, R.sub.2 is a methyl group or an ethyl group, R.sub.3 is a hydrogen atom or a methyl group, n is an integer of 4 to 5 and X is a hydrogen atom or a methyl group.

3. The compound according to claim 1, which is ##STR11##

4. The compound according to claim 1, which is ##STR12##

5. The compound according to claim 1, which is ##STR13##

6. The compound according to claim 1, which is ##STR14##

7. The compound according to claim 1, which is ##STR15##