Arylphosphonodiamide compounds and herbicidal compositions thereof

Abstract

Herbicides have the formula ##STR1## in which R is hydrogen, mono- or poly-halo, mono- or di-(C.sub.1 -C.sub.4 alkyl), C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy, phenoxy or nitro;R.sub.1 is hydrogen or C.sub.1 -C.sub.4 alkyl;R.sub.3 is C.sub.1 -C.sub.6 alkyl;R.sub.2 is C.sub.2 -C.sub.4 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl, optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.4 alkyl and one C.sub.1 -C.sub.4 alkoxy group, phenyl-(C.sub.1 -C.sub.2)alkyl or pyridyl; orR.sub.1 and R.sub.2, and/or R.sub.3 and R.sub.4 respectively, taken together with the nitrogen atom, form a 4-8 member ring, optionally including an oxygen heteroatom;and R.sub.4 is C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl, optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.4 alkyl and one C.sub.1 -C.sub.4 alkoxy group, phenyl-(C.sub.1 -C.sub.2 alkyl) or pyridyl;provided that if R.sub.1 is hydrogen, R.sub.2 is alkyl or cycloalkyl.

Description

FIELD OF THE INVENTION

This invention relates to the use of certain arylphosphonodiamides as herbicides.

Some phosphonodiamide derivatives of herbicidal diphenyl ethers are described in U.S. Pat. No. 4,39,624 of Maier et al. Some herbicidal alkyl phosphonodiamides are disclosed in British Patent 1,350,286 of Nissan Chemical Industries, Ltd. and in Bakumenko et al., Khim. Sel'sk. Khoz., vol. 4, p. 691 (1966).

DESCRIPTION OF THE INVENTION

In one aspect this invention relates to the use as herbicides of certain arylphosphonodiamides which have the formula: ##STR2## in which

R is hydrogen, mono- or poly-halo, mono- or di-(C.sub.1 -C.sub.4 alkyl), C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy, phenoxy or nitro;

R.sub.1 is hydrogen or C.sub.1 -C.sub.4 alkyl; R.sub.3 is C.sub.1 -C.sub.6 alkyl;

R.sub.2 is C.sub.2 -C.sub.4 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl, optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.4 alkyl and one C.sub.1 -C.sub.4 alkoxy group, phenyl-(C.sub.1 -C.sub.2) alkyl or pyridyl; or

R.sub.1 and R.sub.2, and/or R.sub.3 and respectively, taken together with the nitrogen atom, form a 4-8 member ring, optionally including an oxygen heteroatom;

and R is C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl, optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.4 alkyl and one C.sub.1 -C.sub.4 alkoxy group, phenyl-(C.sub.1 -C.sub.2 alkyl) or pyridyl;

provided that if R.sub.1 is hydrogen, R.sub.2 is alkyl or cycloalkyl.

Many of the compounds within the formula above are novel, but some compounds falling within this genus have been disclosed in articles relating to investigations in chemical synthesis or spectroscopy. These include Hoffmann et al, Chem. Ber., vol. 93, p. 861 (1960) and Nielsen et al, J. Chem. Eng. Data, vol. 9, p. 167 (1964).

The novel compounds which form another aspect of this invention have the general formula: ##STR3## in which

R is hydrogen mono- or poly-halo, mono- or di-(C.sub.1 -C.sub.4 alkyl), C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy, phenoxy or nitro;

R.sub.1 is hydrogen or C.sub.1 -C.sub.4 alkyl;

R.sub.3 is C.sub.1 -C.sub.6 alkyl;

R.sub.2 is C.sub.2 -C.sub.4 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl, optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.4 alkyl and one C.sub.1 -C.sub.4 alkoxy group, phenyl-(C.sub.1 -C.sub.2)alkyl or pyridyl; or

R.sub.1 and R.sub.2, and/or R.sub.3 and respectively, taken together with the nitrogen atom, form a 4-8 member ring, optionally including an oxygen heteroatom;

and is R.sub.4 C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl, optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.4 alkyl and one C.sub.1 -C.sub.4 alkoxy group, phenyl-(C.sub.1 -C.sub.2 alkyl) or pyridyl;

provided that if R.sub.1 is hydrogen, R.sub.2 is alkyl or cycloalkyl;

excluding compounds in which

a) R.sub.1 -R.sub.4 are all ethyl or

b) R.sub.2 and R.sub.4 are both phenyl.

The term "alkyl" includes straight and branched chained saturated acyclic hydrocarbyl moieties having the indicated number of carbon atoms. Preferred alkyl groups include methyl, ethyl, n-propyl, isopropyl, n-butyl, sec.-butyl, t-butyl, isobutyl, n-amyl and n-hexyl. The term "cycloalkyl" includes saturated cyclical hydrocarbyl moieties, such as cyclopentyl and cyclohexyl. The terms "halogen" or "halo" include chloro, bromo, fluoro and iodo. Substituted phenyl groups for R.sub.2 and R.sub.4 may contain one or more of the indicated substituents. Preferred substituents are chloro, fluoro, nitro, methyl, ethyl, i-propyl, t-butyl, methoxy, ethoxy and trifluoromethyl.

Preferred compounds of this series include those in which R.sub.1 -R.sub.4 are all alkyl groups, particularly alkyl groups having from 3 to 4 carbon atoms, particularly straight chain groups, such as n-propyl and n-butyl. Most preferred are compounds in which R.sub.1 -R.sub.4, or R.sub.3 and R.sub.4, are n-butyl.

As used herein, the term "herbicide" means a compound or composition which adversely controls or modifies the growth of plants. By the term "herbicidally effective amount" is meant any amount of such compound or composition which causes an adverse modifying effect upon the growth of plants. By "plants", it is meant germinant seeds, emerging seedlings and established vegetation, including roots and above-ground portions. Such controlling or modifying effects include all deviations from natural development, such as killing, retardation, defoliation, desiccation, regulation, stunting, tillering, leaf burn, dwarfing, and the like.

The compounds of this invention have been found to be active herbicides, particularly post-emergent herbicides; i.e. they may be applied to control or kill existing vegetation which has already emerged from the soil. Some of the compounds of this invention have demonstrated such postemergence herbicidal activity in a relatively short time, and against some weeds, with a very strong effect. Herbicides having such rapid and extensive post-emergence activity are sometimes referred to as "contact and burn" or "burn-down" herbicides and are used, among other applications, for clearing vegetation from land such as building lots, highway median strips, railroad track beds, and crop land prior to planting or in minimum till or no-till farming. Some of the compounds of this invention also demonstrate pre-emergence activity, that is, control or killing of vegetation by application prior to the emergence of vegetation from the soil. Pre-emergence herbicides may be applied by techniques such as incorporation into, or spraying or spreading onto, the surface of the soil.

Compounds showing "contact-and-burn" effect, but little or no pre-emergence activity, may be useful in clearing land prior to planting since planting of a crop can be done relatively soon after the herbicide is applied.

The compounds of this invention may be prepared from starting phosphonodichlorides and appropriate amines, in one or two steps, by the general reaction ##STR4## Preferably the two amines are reacted stepwise with the arylphosphonyl dichloride.

Processes of this type in general are carried out at temperatures of from about 0.degree. to about 1 20.degree. C., preferably from about 20.degree. to about 60.degree. C., preferably in the presence of an inert solvent, such as an aromatic hydrocarbon (preferably toluene), dichloromethane or ether. The hydrogen chloride produced during the reaction is generally removed by using a stoichiometric excess of the reactant amine or a stoichiometric amount of a tertiary amine such as triethylamine.

For compounds in which R.sub.1 is not hydrogen, it is preferable to form an intermediate chloroamide by first reacting the phosphonodichloride with an excess of an amine R.sub.1 R.sub.2 NH, and then introducing a second amine R.sub.3 R.sub.4 NH in the form of the salt R.sub.3 R.sub.4 N.sup.-M.sup.+ obtained, for instance, from the amine and an n-alkyllithium.

The following represent examples of preparation of compounds of this invention.

EXAMPLE 1

Preparation of N,N-Dipropyl-N'-(s-butyl) phenylphosohonodiamide

(Compound No. 2)

Phenyl phosphonic dichloride (2.75 g, 14.1 mmol) and di-n-propylamine (1.43 g, 14.1 mmol) were added sequentially to a solution of triethylamine (3.14 g, 30 mmol) in 25 ml of toluene with stirring and cooling in an ice bath, under nitrogen. After 10 minutes, the reaction mixture was stirred at room temperature for 1 hour, filtered, and again cooled. Then, sec.-butylamine (1.03 g., 14.1 mmol) was added and stirring was continued overnight.

The reaction mixture was mixed with water, phase-separated, washed with saturated brine and dried. The solvent was removed, resultant oil was combined with 20 ml hexanes, filtered and again rotary evaporated to yield 3.1 g of an oil. The structure was confirmed by spectroscopic analyses.

EXAMPLE 2

Preparation of N,N,N',N'-tetra-n-butyl-4-methoxyohenylphosohonodiamide

(Compound No. 5)

4-Methoxyphenyl phosphonic dichloride (1.5 g, 6.7 mmol) in a small amount of methylene dichloride was added to di-n-butylamine (3.6 g, 28 mmol) in 50 ml methylene dichloride with stirring at room temperature under nitrogen. Following an additional 30 minutes, the crude product mixture was washed with 5% HCl (until the extracts were acidic) and water. Drying and rotary evaporation gave 2.1 g of a crude yellow oil which was chromatographed. The compound eluting with an R.sub.F of 0.53 (25% ethyl acetate, silica gel 60) was collected and evaporated to yield 0.55 g of intermediate N,N-di-n-butyl-4-methoxyphenylphosphonoamide chloride. This material gave satisfactory spectroscopic analyses.

The intermediate chloroamide was heated with lithium dibutylamide, prepared from dibutylamine (0.32 g, 1.45 eq.) amd n-butyllithium (1.5 ml, 1.6M in hexane), in 5 ml of dry ether with stirring under nitrogen at 0.degree.. After 30 minutes, the crude product mixture was water washed and dried. Rotary evaporation yielded 0.52 g of a yellow oil which was chromatographed over silica gel using 1:1 ethyl acetate-hexanes as the eluent. There was collected 0.30 g of a colorless oil following rotary evaporation. Spectroscopic analysis confirmed the structure as the desired product.

Table I depicts representative compounds of this invention, prepared by one of the processes described above. Most or all these compounds were obtained as oils. Structures were compared by spectroscopic analyses.

TABLE I______________________________________ ##STR5##Cmpd.No. R R.sub.1 R.sub.2 R.sub.3 R.sub.4______________________________________1. H n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.72. H H sec-C.sub.4 H.sub.9 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.73. H CH.sub.3 C.sub.6 H.sub.5 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.74. H CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 C.sub.6 H.sub.55. 4-OCH.sub.3 n-C.sub.4 H.sub.9 n-C.sub.4 H.sub.9 n-C.sub.4 H.sub.9 n-C.sub.4 H.sub.96. H n-C.sub.4 H.sub.9 n-C.sub.4 H.sub.9 n-C.sub.4 H.sub.9 n-C.sub.4 H.sub.97. H C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.58. 3-OCH.sub.3 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.79. H H C.sub.6 H.sub.5 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.710. H i-C.sub.4 H.sub.9 i-C.sub.4 H.sub.9 i-C.sub.4 H.sub.9 i-C.sub.4 H.sub.911. H C.sub.2 H.sub.5 C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.2 H.sub.512. H ##STR6## C.sub.2 H.sub.5 C.sub.2 H.sub.513. H (CH.sub.2).sub.6 C.sub.2 H.sub.5 C.sub.2 H.sub.514. H CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 C.sub.6 H.sub.5 CH.sub.215. H n-C.sub.4 H.sub.9 C.sub.6 H.sub.5 CH.sub.2 n-C.sub.4 H.sub.9 C.sub.6 H.sub.5 CH.sub.216. H CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 C.sub.2 H.sub.5 C.sub.2 H.sub.517. H n-C.sub.4 H.sub.9 C.sub.6 H.sub.5 CH.sub.2 C.sub.2 H.sub.5 C.sub.2 H.sub.518. H C.sub.2 H.sub.5 C.sub.6 H.sub.5 C.sub.2 H.sub.5 C.sub.6 H.sub.519. 2,5-CH.sub.3 n-C.sub.4 H.sub.9 C.sub.6 H.sub.5 CH.sub.2 C.sub.2 H.sub.5 C.sub.2 H.sub.520. 2,5-CH.sub.3 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 C.sub.2 H.sub.5 C.sub.2 H.sub.521. 2,5-CH.sub.3 CH.sub.3 C.sub.6 H.sub.5 CH.sub.2 CH.sub.3 C.sub.6 H.sub.5 CH.sub.222. 4-OCH.sub.3 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.7 n-C.sub.4 H.sub.9 n-C.sub.4 H.sub.923. H C.sub.2 H.sub.5 C.sub.2 H.sub.5 n-C.sub.6 H.sub.13 n-C.sub.6 H.sub.1324. H C.sub.2 H.sub.5 C.sub.6 H.sub.5 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.725. H n-C.sub.4 H.sub.9 C.sub.6 H.sub.5 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.726. H CH.sub.3 2-CH.sub.3 C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.727. H CH.sub.3 3-CH.sub.3 C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.728. H CH.sub.3 4-CH.sub.3 C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.729. H (CH.sub.2).sub.3 n-C.sub.4 H.sub.9 C.sub.6 H.sub.530. H (CH.sub.2).sub.3 C.sub.2 H.sub.5 C.sub.6 H.sub.531. H CH.sub.3 C.sub.6 H.sub.5 n-C.sub.4 H.sub.9 n-C.sub.4 H.sub.932. H CH.sub.3 3-CF.sub.3 C.sub.6 H.sub.4 n-C.sub.3 H.sub.7 n-C.sub.3 H.sub.7______________________________________

Herbicidal Activity Tests

Compounds in Table I were tested for herbicidal activity as follows:

The herbicidal effect was observed by comparing the extent of weed control in test flats treated with the compounds against that occurring in similar non-treated control flats. All were applied at 3.57 lb/A (4 kg/ha) to pre-emergence and post-emergence screening flats. An 80 gal/A (748.3 l/ha) spray volume was utilized. Post-emergence flats were seeded 12 days prior to treatment. Pre-emergence flats were seeded one day prior to treatment. Overhead watering of pre-emergence flats and soil surface watering of post-emergence flats, so as to avoid wetting the foliage, were carried out for the duration of the test.

Weed seeds were planted in a flat at a seed depth of 0.5 inch (1.3 cm). Soil for flats was prepared using loam soil fortified with 17-17-17 fertilizer (N-P.sub.2 O.sub.5 -K.sub.2 O on a weight basis) and Captan 80W fungicide. The test weeds were as follows:

______________________________________COMMON NAME SCIENTIFIC NAME______________________________________green foxtail Setaria viridiswatergrass Echinochloa crusgalliwild oat Avena fatuaannual morning glory Ipomoea purpureavelvetleaf Abutilon theophrastiwild mustard Brassica kabercurly dock Rumex crispus (some compounds)yellow nutsedge Cyperus esculentus______________________________________

The spray solutions were prepared by dissolving 240 mg of test compound in 20 ml of acetone containing 1% polyoxyethylene sorbitan monolaurate emulsifier, then adding 20 ml of water to the resulting solution. The stock solutions were applied using a linear spray table. Pre-emergence flats are raised to the level of the post-emergence foliage canopy by setting the flats on a wooden block.

The degree of weed control was visually assessed and recorded as percentage control compared to the growth of the same species in an untreated check flat of the same age. The rating scale ranges from 0 to 100%, where 0 equals no effect with plant growth equal to the untreated control, and 100 equals complete kill.

Ratings were taken in pre-emergence tests approximately 12-18 days after treatment (DAT). In post-emergence tests, ratings were taken at two intervals. On the sixth day after treatment, overall control was rated, as an indication of total vegetative control, or "contact and burn" activity. Approximately 12-18 days after treatment, the tests were rated for overall post-emergence activity.

Results are listed in Table II below, expressed as average control of the three grassy (GR) (wild oat, watergrass, foxtail) and three broadleaf weeds (BL) (morning glory, mustard, velvetleaf), and of nutsedge (NS).

TABLE II__________________________________________________________________________% Control, 3.57 kg/haPre-emergence Post-emergenceCompound 12-18 DAT 6 DAT 12-18 DATNo. GR avg. BL avg. NS GR avg. BL avg. NS GR avg. BL avg. NS__________________________________________________________________________1. 0 0 0 10 30 0 33 50 02. 0 0 0 30 90 0 67 100 03. 0 0 0 30 50 10 33 53 04. 0 0 0 10 30 0 0 73 05.*** 0 0 0 -- -- -- 18 44 156. 0 0 0 -- -- -- 67 100 07. 0 0 0 20 80 0 43 100 08. 0 0 0 20 90 5 62 98 109. 0 0 0 25 60 0 0 83 010. 0 0 0 -- -- -- 0 26 011. 0 0 0 -- -- -- 52 63 012. 0 0 0 -- -- -- 13 23 013. 0 0 0 -- -- -- 30 50 014. 0 0 0 -- -- -- 18 56 015. 0 0 0 -- -- -- 0 28 016. 0 0 0 -- -- -- 7 19 017. 0 0 0 -- -- -- 33 38 018. 0 0 0 -- -- -- 0 29 019. 0 0 0 -- -- -- 47 5 020. 0 0 0 -- -- -- 62 50 021. 0 0 0 -- -- -- 49 44 022.* 8 28 0 60 100 25 6 100 523.* 0 38 0 60 95 15 10 100 524.* 0 30 0 65 98 15 13 100 525.* 0 36 0 40 90 10 6 86 026.* 0 10 0 30 85 5 41 76 527.* 0 13 0 30 85 0 26 80 028.** 0 13 0 30 85 5 26 76 029.* 0 0 0 30 85 10 5 83 530.* 0 41 0 30 90 5 21 80 531.* 0 25 0 30 85 5 15 83 032.* 0 15 0 20 75 5 28 83 5__________________________________________________________________________ *Application rate: 4 kg/ha **Application rate: 2 kg/ha ***Application rate: 1.5 kg/ha

Selected compounds were further tested against the same weeds at a lower application rate of 1.5 kg/ha. In general, control of grassy weeds was lower, but for the most part, control of broadleaf weeds remained at 80% or above.

In practice, a pure compound can be used as a herbicide. However, in general, the compounds are first formulated with one or more inert carriers or diluents suitable for herbicidal use, before being applied.

The compositions or formulations, including a compound as described herein, may exist in any one of a number of solid or liquid forms. Examples of liquid forms are emulsifiable concentrates, flowables and pastes. Such compositions may contain, in addition to the active compound or compounds, various carriers or diluents; surface active agents (wetting agents, dispersing agents and/or emulsifying agents); solvents (water, or organic solvents such as aromatic solvents or chlorinated aliphatic solvents); adhesives; thickeners; binders; antifoaming agents; and other substances as mentioned herein. Solid carriers or diluents included in such compositions or formulations may include, for example, ground natural minerals such as kaolins, alumina, calcium carbonate, silica, kieselguhr, clay, etc.; ground synthetic minerals such as various silicates and aluminosilicates and ground vegetable products such as bark, cornmeal, sawdust, cellulose powder and the like.

To manufacture solid compositions, the active substances are mixed with solid carriers or diluents such as those mentioned above and the mixture is ground to the appropriate size. Granules can be manufactured by dissolving an active compound in an organic solvent and applying the mixture, for example, by atomization, onto an absorptive granulated inert material, such as silica. Adhesives may be utilized to assist in the incorporation of the compound onto the solid particles. Pellets or granules can be manufactured by extrusion with appropriate carriers and binders.

Wettable powders, flowables, and pastes are obtained by mixing and grinding an active compound with one or more dispersing agents and/or solid carriers or diluents. Also included may be wetting agents and/or dispersing agents, for example, lignins, methyl cellulose, naphthalenesulfonic acid derivatives, fatty alcohol sulfates and various types of alkali and alkaline earth metal salts of fatty acids.

Emulsifiable concentrates are generally obtained by dissolving the active compound in an organic solvent, for example, butanol, cyclohexanone, xylenes, or higher boiling aromatic hydrocarbons. To obtain suspensions or emulsions in water wetting agents are generally also added.

The compositions may also be used in the form of microcapsules. Microcapsules consist of fully enclosed or encapsulated droplets or granules containing the active compound, enclosed within an inert porous membrane, so as to permit escape of the encapsulated material into the surrounding medium or environment at a controlled rate.

Useful encapsulating materials include natural and synthetic rubbers or latexes, cellulosic materials, styrenebutadiene copolymers, polyacrylonitriles, polyacrylates, polyesters, polyamides, polyurethanes and starch xanthates.

It is possible to use highly concentrated liquid compositions containing up to about 95% by weight of the active compound, or even the active compound alone for those compounds which are liquids, when applying the compound in the form of a finely divided liquid by use of various atomizing equipment, for example by airplane crop-spraying techniques. For other purposes, however, the various types of compositions which can be utilized for these compounds will contain varying amounts of the compound according to the type of composition and the intended use.

In general, compositions may contain from 0.1 to 95% of the active compound, more preferably from 0.5 to 90%. Some typical compositions will contain an active compound as follows: Wettable powders, flowables and pastes--20 to 90% active compound; oil suspensions, emulsions, solutions and emulsifiable concentrates--5 to 90% active compound; aqueous suspensions--10 to 50% active compound; dusts and powders--1 to 25% active compound; granules and pellets--1 to 20% active compound.

The rate of application of the active compound to a locus to be controlled will depend on the activity of the compound and/or composition and the nature of the seeds and plants to be controlled and will vary from about 0.05 to about 50 pounds per acre (about 0.06 to about 56 kg/ha).

Compositions containing one or more of the active compounds described, in a herbicidally effective amount, may be applied to the plant or locus to be controlled in any conventional manner. Thus, powders and various liquid compositions containing the active compound can be applied by the use of power dusters, boom and hand sprayers and spray spray dusters, or applied from airplanes as mists or sprays. When applied in the latter method, they may be effective in very low dosages. To modify or control growth of germinating seeds or emerging seedlings, liquid compositions may be applied to the soil with conventional methods and may be distributed in the soil to a depth of one-half inch below the soil surface. The compositions need not be admixed with the soil particles, but can be applied merely by sprinkling on the surface of the soil.

Compositions including active compounds may also be applied by addition to irrigation waters supplied to the field to be treated. This method of application permits penetration of the compounds into the soil as the water is absorbed therein.

______________________________________EXAMPLES OF TYPICAL COMPOSITIONS______________________________________Ingredient Weight %______________________________________OilActive Compound 1Oil solvent-heavy aromatic naphtha 99Total 100Emulsifiable ConcentrateActive Compound 50Kerosene 45Emulsifying agent (mixture of long 5chain ethoxylated polyethers withlong chain sulfonate)Total 100Emulsifiable ConcentrateActive Compound 90Kerosene 5Emulsifying agent (mixture of long 5chain ethoxylated polyethers withlong chain sulfonate)Total 100Dusts and/or PowdersIngredient Wt. % Wt. % Wt. %______________________________________Active Compound 0.5 50.0 90.0Attapulgite Clay Powder 93.5 44.0 4.0Sodium lignin sulfonate 5.0 5.0 5.0Sodium dioctyl sulfosuccinate 1.0 1.0 1.0TOTAL 100.0 100.0 100.0______________________________________

The compositions of the invention may comprise, in addition to one or more compounds of the invention, one or more compounds not of the invention but which possess biological activity. Compounds not of this invention may be other pesticidal agents, such as herbicides, fungicides, insecticides, acaricides, nematocides, bactericides, and plant growth regulators. Such compositions may also contain soil disinfectants or fumigants and may further contain fertilizers, thus making it possible to provide multi-purpose compositions containing one or more of the compounds described herein as well as, optionally, other pesticides and also fertilizers, all intended and formulated for use at the same locus. Accordingly, in yet a still further embodiment, the invention provides an herbicidal composition comprising a mixture of at least one herbicidal compound of formula (I) as hereinbefore defined with at least one other herbicide.

The other herbicide may be any herbicide not having the formula (I). It will generally be an herbicide having a complementary action in the particular application.

Examples of useful complementary herbicides include:

A. Benzo-2,1,3-thiodiazin-4-one-2,2-dioxides such as 3-isopropylbenzo-2,1,3-thiadiazin-4-one-2,2-dioxide (bentazone);

B. hormone herbicides, particularly the phenoxy alkanoic acids such as 4-chloro-2-methylphenoxyacetic acid (MCPA), S-ethyl 4-chloro-O-tolyloxy thioacetate (MCPA-thioethyl), 2-(2,4-dichlorophenoxy) propionic acid (dichlorprop), 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), 4-(4-chloro-2-methylphenoxy)butyric acid (MCPB), 2,4-dichlorophenoxyacetic acid (2,4-D), 4-(2,4-dichlorophenoxy)butyric acid (2,4-DB), 2-(4-chloro-2-methylphenoxy) propionic acid (mecoprop), 3,5,6-trichloro-2-pyridyloxyacetic acid (trichlopyr), 4-amino-3,5-dichloro-6-fluoro-2-pyridyloxyacetic acid (fluroxypyr), 3,6-dichloropyridine-2-carboxylic acid (clopyralid), and their derivatives (e.g. salts, esters and amides);

C. 1,3-dimethylpyrazole derivatives such as 2-[4-(2,4-dichlorobenzoyl) 1,3-dimethylpyrazol-5-yloxy] acetophenone (pyrazoxyfen), 4-(2,4-dichlorobenzoyl)1,3-dimethylpyrazol-5-yltoluene sulfonate (pyrazolate) and 2-[4-(2,4-dichloro-m-toluolyl)-1,3-dimethylpyrazol-5-yloxy]-4,-methylacetophenone (benzofenap);

D. Dinitrophenols and their derivatives (e.g. acetates such as 2-methyl-4,6-dinitrophenol (DNOC), 2-t-butyl-4,6-dinitrophenol (dinoterb), 2-sec.-butyl-4,6-dinitrophenol (dinoseb) and its ester, dinoseb acetate;

E. dinitroaniline herbicides such as N',N'-diethyl-2,6-dinitro-4-trifluoromethyl-m-phenylenediamin (dinitramine), 2,6-dinitro-N,N-dipropyl-4-trifluoromethylaniline (trifluralin), N-ethyl-N-(2-methylallyl)-2,6-dinitro-4-trifluoromethylaniline (ethalfluralin), N-(1-ethylpropyl)-2,6-dinitro-3,4-xylidine (pendimethalin); and 3,5-dinitro-N.sup.4, N.sup.4 -dipropylsulphanilamide (oryzalin);

F. arylurea herbicides such as N'-(3,4-dichlorophenyl)-N,N-dimethylurea (diuron), N,N-dimethyl-N'-[3-(trifluoromethyl) phenyl]urea (flumeturon), 3-(3-chloro-4-methoxyphenyl)1,1-dimethylurea (metoxuron), 1-butyl-3-(3,4-dichlorophenyl)-1-methylurea (neburon), 3-(4-isopropylphenyl)-1,1-dimethylurea (isoproturon), 3-(3-chloro-p-tolyl)-1,1-dimethylurea (chlorotoluron), 3-[4-(4-chlorophenoxy) phenyl]-1,1-dimethylurea (chloroxuron), 3-(3,4-dichlorophenyl)-1-methylurea (linuron), 3-(4-chlorophenyl)-1-methoxy-1-methylurea (monolinuron), 3-(4-bromo-4-chlorophenyl)-1-methoxy-1-methylurea (chlorobromuron), i-(1-methyl-1-phenylethyl)-3-p-tolylurea (daimuron), and 1-benzothiazol-2-yl-1,3-dimethylurea (methabenzthiazuron);

G. phenylcarbamoyloxyphenylcarbamates such as 3-[methoxycarbonylamino]phenyl (3-methylphenyl)carbamate (phenmedipham) and 3-[ethoxycarbonylamino]-phenyl phenylcarbamate (desmedipham);

H. 2-phenylpyridazin-3-ones such as 5-amino-4-chloro-2-phenylpyridazin-3-one (chloridazon), and 4-chloro-5-methylamino-2-(.alpha.,.alpha.,.alpha.-trifluoro-m-tolyl) pyridazin-3(2H)-one (norflurazon);

I. uracil herbicides such as 3-cyclohexyl-5,6-trimethyleneuracil (lenacil), 5-bromo-3-sec.-butyl-6-methyluracil (bromacil) and 3-t-butyl-5-chloro-6-methyl-uracil (terbacil);

J. triazine herbicides such as 2-chloro-4-ethyl amino-6-(i-propylamino)-1,3,5-triazine (atrazine), 2-chloro-4,6-di(ethylamino)-1,3,5-triazine (simazine), 2-azido- 4-(i-propylamino)-6-methylthio-1,3,5-triazine (aziprotryne), 2-(4-chloro-6-ethylamino-1,3,5-triazin-2-ylamino)-2- methylpropionitrile (cyanazine), N.sup.2, N.sup.4 -di-isopropyl-6-methylthio-1,3,5-triazine-2,4-diamine (prometryn), N.sup.2 -(1,2-dimethylpropyl)-N.sup.4 -ethyl-6-methylthio-1,3,5-triazine-2,4-diamine (dimethametryn), N.sup.2,N.sup.4 -diethyl-6-methylthio-1,3,5-triazine-2,4-diamine (simetryne), and N.sup.2 -tert.-butyl-N.sup.4 -ethyl-6-methylthio-1,3,5-triazine-2,4-diamine (terbutryn);

K. phosphorothioate herbicides such as S-2-methyl-piperidinocarbonyl-methyl O,O-dipropyl phosphorodithioate (piperophos), S-2-benzenesulphonamidoethyl O,O-diisopropyl phosphonodithioate (bensulide), and O-ethyl O-6-nitro-m-tolyl sec.-butylphosphoramidothioate (butamifos);

L. thiolcarbamate herbicides such as S-ethyl N-cyclohexyl-N-ethyl thiocarbamate (cycloate), S-propyl dipropyl-thiocarbamate (vernolate), S-ethyl-azepine-1-carbothioate (molinate), S-4-chlorobenzyl diethylthiocarbamate (thiobencarb), S-ethyl di-isobutyl-thiocarbamate (butylate)*, S-ethyl di-isopropylthiocarbamate (EPTC)*, S-2,3,3-trichloroallyl diisopropyl thiocarbamate (triallate), S-2,3-dichloroallyl diisopropyl thiocarbamate (diallate), S-benzyl 1,2-dimethylpropyl (ethyl) thiocarbamate (esprocarb), S-benzyl di(sec.-butyl) thiocarbamate (tiocarbazil), 6-chloro-3-phenylpyridazin-4-yl S-octyl thiocarbamate (pyridate), and S-1-methyl-1-phenylethylpiperidine-1-carbothioate (dimepiperate);

*These compounds are preferably employed in combination with a safener such as 2,2-dichloro-N,N-di-2-propenylacetamide (dichlormid).

M. 1,2,4-triazin-5-one herbicides such as 4-amino-4,5-dihydro-3-methyl-6-phenyl-1,2,4-triazine-5-one (metamitron) and 4-amino-6-butyl-4,5-dihydro-3-methylthio-1, 3,4-triazin-5-one (metribuzin);

N. benzoic acid herbicides such as 2,3,6-trichlorobenzoic acid (2,3,6-TBA), 3,6-dichloro-2-methoxybenzoic acid (dicamba) and 3-amino-2,5-dichlorobenzoic acid (chloramben);

O. anilide herbicides such as 2-chloro-2',6'-diethyl-N-(2-propoxyethyl)acetanilide (pretilachlor), N-butoxymethyl-2-chloro-2',6,-diethylacetanilide (butachlor), the corresponding N-methoxy compound (alachlor), the corresponding N-i-propyl compound (propachlor), 3',4'- dichloropropionanilide (propanil), 2-chloro-N-[pyrazol-1-ylmethyl]acet-2,-6,xylidide(metazachlor), 2-chloro-6'-ethyl-N-(2-methoxy-1-methylethyl) acetotoluidide (metolachlor), 2-chloro-N-ethoxymethyl-6'-ethylacetotoluidide (acetochlor), and 2-chloro-N-(2-methoxyethyl)acet-2',6'-xylidide (dimethachlor);

P. dihalobenzonitrile herbicides such as 2,6-dichlorobenzonitrile (dichlobenil), 3,5-dibromo-4-hydroxy-benzonitrile (bromoxynil) and 3,5-diiodo-4-hydroxy-benzonitrile (ioxynil);

Q. haloalkanoic herbicides such as 2,2-dichloropropionic acid (dalapon), trichloroacetic acid (TCA) and salts thereof;

R. diphenylether herbicides such as ethyl 2-[5-(2-chloro-trifluoro-p-tolyloxy)-2-nitrobenzoyl]oxy propionate (lactofen), D-[5-(2-chloro-.alpha.,.alpha.,.alpha.-trifuoro-p-tolyl)-2-nitrobenzoyl] gycolic acid (fluroglycofen) or salts or esters thereof, 2,4-dichlorophenyl-4-nitrophenyl ether (nitrofen), methyl-(2,4-dichlorophenoxy)-2-nitrobenzoate (bifenox), 2-nitro-5-(2-chloro-4-trifluoromethyl-phenoxy) benzoic acid (acifluorfen) and salts and esters thereof, 2-chloro-4-trifluoromethylphenyl 3-ethoxy-4-nitrophenyl ether (oxyfluorfen) and 5-[2-chloro-4-(trifluoromethyl)phenoxy]-N-(methylsulfonyl)-2-nitrobenzamide (fomesafen); 2,4,6-trichlorophenyl 4-nitrophenyl ether (chlornitrofen) and 5-(2,4-dichlorophenoxy)-2-nitroanisole (chlomethoxyfen);

S. phenoxyphenoxypropionate herbicides such as (RS)-2-[4-(2,4-dichlorophenoxy) phenoxy]propionic acid (diclofop) and esters thereof such as the methyl ester, 2-[4-(5-trifluoromethyl)-2-(pyridinyl)oxy]phenoxypropanoic acid (fluazifop) and esters thereof, 2-[4-(3-chloro-5-trifluoromethyl)-2-pyridinyl)oxy] phenoxypropanoic acid (haloxyfop) and esters thereof, 2-[4-(6-chloro-2-quinoxalinyl)oxy] phenoxypropanoic acid (quizalofop) and esters thereof and (.+-.)-2-[4-(6-chlorobenzoxazol-2-yloxy)phenoxy] propionic acid (fenoxaprop) and esters thereof such as the ethyl ester;

T. cyclohexanedione herbicides such as 2,2-dimethyl-4,6-dioxo-5-[1-(2-propenyloxyimino)butyl] cyclohexane carboxylic acid (alloxydim) and salts thereof, 2-(1-ethoxyimino) butyl-5-[2-(ethylthio)-propyl]-3-hydroxy-2-cyclohexan-1-one (sethoxydim), 2-(1-ethoxyimino)butyl-3-hydroxy-5-thian-3 -ylcyclohex-2-enone (cycloxydim), 2-[1(ethoxyimino)propyl]-3-hydroxy-5-mesitylcyclohex-2-enone (tralkoxydim), and (.+-.)-2-(E)-1-[(E)-3-chloroallyloximino] propyl-5-[2-(ethylthio)propyl]-3-hydroxycyclohex-2-enone (clethodim);

U. sulfonyl urea herbicides such as 2-chloro-N (4-methoxy-6-methyl-1, 3,5-triazin-2-yl)-aminocarbonyl) benzenesulphonamide (chlorosulfuron), methyl 2-[([(4,6-dimethyl2-pyrimidinyl)amino]-carbonyl)amino]-sulphonylbenzoic acid (sulfometuron), 2-([(3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbonyl]amino)-sulphonyl)benzoic acid (metsulfuron) and esters thereof; -(4,6-dimethoxypyrimidin-2-ylcarbamoylsuphamoly)-O-toluic acid (benzsulfuron) and esters thereof such as the ester thereof methyl, 3-[3-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)ureido- sulphonyl]thiophene-2-carboxylate (DPX-M6313), 2-(4-chloro-6-methoxy pyrimidin-2-yl carbamoylsulphamoyl benzoic acid (chlorimuron) and esters such as the ethyl ester thereof, 2-(4,6-dimethoxypyrimidin-2-ylcarbamoylsulphamoyl)-N,N-dimethyl-nicotinamide, 2-[4,6-bis(difluoromethoxy)pyrimidin-2-ylcarbamoylsulphamoyl] benzoic acid (pirimisulfuron) and esters such as the methyl ester thereof, 2-[3-(4-methoxy-6-methyl-1,3,5-triazin-zyl)-3-methylureidosulphonyl] benzoic acid esters such as the methyl ester thereof (DPX-LS300) and 5-(4,6-dimethoxypyrimidin-2-ylcarbamoylsulphamoyl)-1-methylpyrazole-4-carboxylic acid (pyrazosulfuron);

V. imidazolidinone herbicides such as 2-(4,5-dihydro-4-isopropyl-4-methyl-5-oxoimidazol-2-yl) quinoline-3-carboxylic acid (imazaquin), methyl 6-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-m-toluate and p-toluate isomer (imazamethabenz), 2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) nicotinic acid (imazapyr) and isopropylammonium salts thereof, (RS)-5-ethyl-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl) nicotinic acid (imazethapyr);

W. arylanilide herbicides such as benzoyl-N-(3-chloro-4-fluorophenyl)-L-alanine (flamprop) and esters thereof, ethyl N-benzoyl-N-(3,4-dichlorophenyl)-DL-alaninate (benzoylprop-ethyl), N-(2,4-difluorophenyl)-2-(3-trifluoromethyl)phenoxy-3-pyridinecarboxamide (diflufenican);

X amino acid herbicides such as N-(phosphonomethyl)-glycine (glyphosate) and DL-homoalanin-4-yl (methyl) phosphinic acid (gluyfosinate) and their salts and esters, trimethylsulfonium N-(phosphonomethyl)-glycine (sulphosate), and bilanafos;

Y. organoarsenical herbicides such as monosodium methanearsonate (MSMA);

Z. herbicidal amide derivative such as (RS)-N,N-diethyl-2-(1-naphthyloxypropionamide) (napropamide), 3,5-dichloro-N-(1,1-dimethylpropynyl)benzamide (propyzamide), (R)-1-(ethylcarbamoyl)ethyl carbanilate (carbetamide), N-benzyl-N-isopropylpivalamide (tebutam), (RS)-2-bromo-N-(.alpha.,.alpha.-dimethylbenzyl)-3,3-dimethylbutyramide (bromobutide), N-[3-(1-ethyl-1-methylpropyl)-isoxazol-5-yl] 2,6-dimethoxybenzamide, (isoxaben), N-phenyl-2-(2-naphthyloxy) propionamide (naproanilide), N,N-dimethyl-diphenylacetamide (diphenamid), and N-(1-naphthyl)phthalamic acid (naptalam);

AA. miscellaneous herbicides including 2-ethoxy-2,3-dihydro-3,3-dimethylbenzofuran methanesulfonate (ethofumesate), 7-oxabicyclo (2.2.1)heptane,1-methyl-4-(1-methylethyl)-2-(2-methylphenylmethoxy)-exo (cinmethylin), 1,2-dimethyl-3,5-diphenylpyrazolium ion (difenzoquat) and salts thereof such as the methyl sulfate salt, 2-(2-chlorobenzyl)-4,4-dimethyl-1,2-oxazoldin-3-one (clomazone), 5-tert.-butyl-3-(2,4-dichloro-5-isopropoxyphenyl)-1,3,4-oxadiazol-2(3H)-one (oxadiazon), 3,5-dibromo-4-hydroxy benzaldehyde 2,4-dinitrophenyloxime (bromofenoxim), 4-chlorobut-2-ynyl-3-chlorocarbanilate (barban), (RS)-2-(3,5-dichlorophenyl)-2-(2,2,2-trichloroethyl)oxirane (tridiphane), (3RS,4RS;3RS,4SR)-3-chloro-4-chloromethyl-1-.alpha.,.alpha.-.alpha.-trifluro-m-tolyl-2-pyrrolidone (in the ratio 3:1) (flurochloridone), dichloroquinoline 8-carboxylic acid (quinchlorac) and 2-(1,3-benzothiazol-2-yl-oxy)-N-methylacetanilide (mefanacet);

BB. examples of useful contact herbicides include bipyridylium herbicides such as those in which the active entity is the 1,1'-dimethyl-4,4'-dipyridylium ion (paraquat) and those in which the active entity is the 1,1-ethylene-2,2,-dipyridylium ion (diquat).

Claims

1. A compound having the formula ##STR7## in which R is hydrogen, mono- or poly-halo, mono- or di-(C.sub.1 -C.sub.4 alkyl), C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy or nitro;

R.sub.1 is hydrogen or C.sub.1 -C.sub.4 alkyl;

R.sub.3 is C.sub.1 -C.sub.6 alkyl;

R.sub.2 is C.sub.2 -C.sub.4 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.4 alkyl and one C.sub.1 -C.sub.4 alkoxy group, phenyl-(C.sub.1 -C.sub.2) alkyl or pyridyl; or

R.sub.1 and R.sub.2, or R.sub.3 and R.sub.4 respectively, taken together with the nitrogen atom, form a 4-8 member ring, optionally including an oxygenhetero atom;

and R is C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.6 alkyl and one C.sub.1 -C.sub.4 alkoxy group; phenyl-(C.sub.1 -C.sub.2 alkyl) or pyridyl;

provided that:

(i) if R.sub.1 is hydrogen, R.sub.2 is alkyl or cycloalkyl; and

(ii) if R is hydrogen or mono- or dialkyl, then R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are not all alkyl; and

excluding compounds in which

a) R.sub.1 -R.sub.4 are all ethyl;

b) R.sub.2 and R.sub.4 are both phenyl; or

c) R.sub.3 and R.sub.4 are both methyl.

2. A compound according to claim 1 in which R is hydrogen.

3. A compound according to claim 1 in which R is methoxy.

4. A compound according to claim 1 in which R.sub.1 -R.sub.4 are all alkyl groups.

5. A compound according to claim 4 in which R.sub.1 -R.sub.4 are all C.sub.3 -C.sub.4 alkyl groups.

6. A compound according to claim 4 in which R is methoxy.

7. A compound according to claim 6 in which R.sub.3 and R.sub.4 are both n-butyl.

8. A compound according to claim 6 in which R.sub.1 -R.sub.4 are all n-butyl.

9. A compound according to claim 6 in which R.sub.1 -R.sub.4 are all n-propyl.

10. A compound according to claim 1 in which R and R.sub.1 are both hydrogen, R.sub.2 is sec.-butyl and R.sub.3 and R.sub.4 are both n-propyl.

11. A compound according to claim 1 in which R is 3-methoxy and R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are each n-propyl.

12. A compound according to claim 1 in which R is 4-methoxy, R.sub.1 and R.sub.2 are both n-propyl and R.sub.3 and R.sub.4 are both n-butyl.

13. A compound according to claim 1 in which R is hydrogen, R.sub.1 is ethyl, R.sub.2 is phenyl, and R.sub.3 and R.sub.4 are both n-propyl.

14. A compound according to claim 1 in which R is hydrogen, R.sub.1 is n-butyl, R.sub.2 is phenyl, and R.sub.3 and R.sub.4 are both n-propyl.

15. A compound according to claim 1 in which R is hydrogen, R.sub.1 and R.sub.2 taken together are trimethylene, R.sub.3 is n-butyl and R.sub.4 is phenyl.

16. A method of controlling undesirable vegetable comprising applying to said vegetation or the locus thereof an herbicidally effective amount of a compound having the formula ##STR8## in which R is hydrogen, mono- or poly-halo, mono- or di-(C.sub.1 -C.sub.4 alkyl), C.sub.1 -C.sub.4 alkoxy, C.sub.1 -C.sub.4 haloalkoxy, phenoxy or nitro;

R.sub.1 is hydrogen or C.sub.1 -C.sub.4 alkyl;

R.sub.3 is C.sub.1 -C.sub.6 alkyl;

R.sub.2 is C.sub.2 -C.sub.4 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl, optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.6 alkyl and one C.sub.1 -C.sub.4 alkoxy group, phenyl-(C.sub.1 -C.sub.2)alkyl or pyridyl; or

R.sub.1 and R.sub.2, or R.sub.3 and R.sub.4 respectively, taken together with the nitrogen atom, form a 4-8 member ring, optionally including an oxygen hetero atom;

and R.sub.4 is C.sub.1 -C.sub.6 alkyl, C.sub.3 -C.sub.6 cycloalkyl, phenyl optionally substituted by C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 haloalkyl, C.sub.1 -C.sub.4 haloalkoxy, one or more halogens, or two C.sub.1 -C.sub.4 alkoxy groups, or one C.sub.1 -C.sub.4 alkyl and one C.sub.1 -C.sub.4 alkoxy group; phenyl-(C.sub.1 -C.sub.2 alkyl) or pyridyl;

provided that if R.sub.1 is hydrogen, R.sub.2 is alkyl or cycloalkyl.

17. A method according to claim 16 in which the compound is applied subsequent to the emergence of the vegetation at the locus.

18. A method according to claim 16 in which R is hydrogen.

19. A method according to claim 16 in which R is methoxy.

20. A method according to claim 16 in which R.sub.1 -R.sub.4 are all alkyl groups.

21. A method according to claim 20 in which R.sub.1 -R.sub.4 are all C.sub.3 -C.sub.4 alkyl groups.

22. A method according to claim 21 in which R is hydrogen or methoxy.

23. A method according to claim 22 in which R.sub.3 and R.sub.4 are both n-butyl.

24. A method according to claim 22 in which R.sub.1 -R.sub.4 are all n-butyl.

25. A method according to claim 22 in which R.sub.1 -R.sub.4 are all n-propyl.

26. An herbicidal composition comprising a) an herbicidally effective amount of a compound according to claim 1; and b) an inert diluent carrier suitable for use with herbicides.