USRE32316E - Substituted phenoxybenzoic acids and derivatives thereof - Google Patents
Substituted phenoxybenzoic acids and derivatives thereof Download PDFInfo
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- USRE32316E USRE32316E US06/075,369 US7536979A USRE32316E US RE32316 E USRE32316 E US RE32316E US 7536979 A US7536979 A US 7536979A US RE32316 E USRE32316 E US RE32316E
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- nitro
- benzoate
- compound
- ammonium
- dichlorophenoxy
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/49—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
- C07C205/57—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C205/59—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms
Definitions
- This invention is concerned with certain phenoxybenzoic acid salts and their use as herbicides.
- This invention provides the method for controlling plant growth that comprises applying an herbicidal amount of an herbicidal compound having the formula: ##STR1## wherein X is halogen, n is 1 to 5, and M is alkali metal (Li, Na, K), alkaline earth metal (Ca, Mg, Ba, Sr), transition metal (e.g.
- the compounds of this invention are readily prepared by the Ullmann ether synthesis reaction between the alkali metal (Na, K) salt of a halophenol and a 5-halo (Cl, Br)-2-nitrobenzoic acid or an ester, amide, or salt thereof.
- the 5-halo-2-nitrobenzoic acid is readily prepared by nitrating a m-halotoluene, followed by oxidation of the methyl group by well-known procedures.
- the salts of this invention are prepared from the halophenoxybenzoic acid, using well known salt forming procedures.
- the salts contemplated herein include metal salts, ammonium salts, and amine salts.
- the metal salts are the alkali metal salts (Li, Na, K); alkaline earth metal salts (Ca, Mg, Ba, etc.); and transition metal salts (Cu, Fe, etc.).
- the amine salts contemplated include salts of primary amines, secondary amines, tertiary amines, aryl amines, and heterocyclic amines.
- the primary amines can have 1-30 carbon atoms and can be saturated or unsaturated straight chain, branched chain, or cyclic.
- Non-limiting examples of primary amines are methylamine; ethylamine; n-propylamine; isopropylamine; n-butylamine; dodecylamine; triacontylamine; allylamine; 2-propynylamine; cyclohexylamine; propargylamine; isobutylamine; sec-butylamine; 2-ethylamine; cyclopropylmethylamine; t-butylamine; 1,1-dimethyl-2-propynylamine; 1,1-diethyl-2-propynlamine, tallow amine (E.G. Armeen I), 2,2-diethyl-2-dimethoxy ethylamine; 1-ethylnylcyclohexylamine and benzylamine.
- the secondary amines can have 2-30 carbon atoms and can be saturated or unsaturated, straight chain, branched chain, or cyclic.
- Non-limiting examples of secondary amines are dimethylamine, diethylamine, dibutylamine, dioctylamine, ditetradecylamine, diallylamine, di-2-hexenylamine, dicyclohexylamine, methylethylamine, methyl cyclohexylamine, diisopropylamine, diisopentylamine, ethyl cyclohexylamine, (3-aminopropyl)alkenylamine wherein the alkenyl group has 16 to 18 carbon atoms; (3-aminopropyl)alkenylamine wherein the alkenyl group has 18, 20 and 22 carbon atoms; and dihydrogenated tallow amine (e.g. Armeen 2HT).
- Armeen 2HT dihydrogenated tallow amine
- the tertiary amines can have 3-30 carbon atoms and can be saturated or unsaturated, straight chain, branched chain, or cyclic.
- Non-limiting examples of tertiary amines are trimethylamine, dimethyl ethylamine, triethylamine, tributylamine, trioctylamine, triallylamine, triisopentylamine, tricyclohexylamine, dimethyl octylamine, n-hexadecyldimethylamine (e.g. Armeen DM16D), n-octadecyldimethylamine (e.g. Armeen DM18D), methyl di-hydrogenated tallowamine (e.g. Armeen M2HT), and methyl di-cocoamine (e.g. Armeen M2C).
- Non-limiting examples of arylamines are aniline; 2-chloroaniline; 3-chloroaniline; 4-chloroaniline; 2-methyl-4-chloroaniline; 2,4-dichloroaniline; 3,4-dichloroaniline; 2,6-dichloro-4-nitroaniline; m-trifluoromethylaniline; isopropylaniline; p-methoxyaniline; N-methoxymethyl-2,6-diethylaniline; ⁇ -naphthylaniline; N-sec-butyl-4-t-butyl-2,6-dinitroaniline; 3-amino-2,5-dichlorobenzoic acid; N,N-dipropyl ⁇ , ⁇ , ⁇ -trifluoro-2,6-dinitro-p-toluidine; 4-bromo-3-chloroaniline;4(4'-chlorophenoxy)aniline; N 3 , N 3 -diethyl-2,
- heterocyclic amines are 3-amino-1,2,4-triazole; 2-chloro-4-ethylamino-6-isopropylamino-s-triazine; pyridine; piperidine; piperazine; morpholine; 4,4'-dipyridyl; 8-hydroxyquinoline; 4-amino-6-t-butyl--(methylthio)-1,2,4-triazine-5(4H)-one; 6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline; indole; hexahydro-1H-azepine; 4-amino-5-chloro-2-phenyl-3(2H)-pyridazinone; pyrrole; imidazolidine; isoquinoline; 2,4-lutidine; 2-methyl-5-ethylpyridine; 2-dimethyl aminopyridine; ⁇ -picoline; ⁇ -picoline; ⁇ -picoline; quinoline
- Non-limiting examples of other salt-forming amino compounds contemplated are 2-chloroethyl dimethylamine; diethanolamine; quanidine; dodecylguanidine; 3-(4-chloro-phenyl)-1,1-dimethylurea; 3-(3,4-dichlorophenyl)-1,1-dimethylurea; Fenuron; Tandex ⁇ -alanine; methyl glycine; glycinamide; aminoacetonitrile; aminoethanthiol; aminoacetic acid; diethyl ethanolamine; diethylenetriamine; isopropanolamine; diisopropanolamine; triisopropanolamine; ethylenediamine; hexamethylenetetramine; hydrazine; phenothiazine; sulfanilic acid; tetraethylenepentamine; thiourea; urea; triethanolamine; triethylenetetramine; diethanol soyaamine (e.g
- Example 1 The ester of Example 1 was hydrolyzed to the corresponding acid and, using known salt-forming methods, salt compounds within the scope of this invention were prepared.
- A represents a 2-nitro-5-(2',4'-dichlorophenoxy)benzoate group
- B represents a 2-nitro-5-(2',4',6'-trichlorophenoxy) benzoate group
- C represents a 2-nitro-5-(2',4'-dichloro-6'-fluorophenoxy)benzoate
- D represents a 2-nitro-5-(2'-chloro-4'-fluorophenoxy)benzoate
- the compounds of this invention can be applied in various ways to achieve herbicidal action. They can be applied per se, as solids or in vaporized form, but are preferably applied as the toxic components in pesticidal compositions of the compound and a carrier. These compositions are preferably applied directly to the soil and incorporated therewith.
- the compositions can be applied, as granulars or dusts; as liquid sprays, or as gas-propelled sprays and can contain, in addition to a carrier, additives such as emulsifying agents, binding agents, gases compressed to the liquid state, odorants, stabilizers, and the like.
- additives such as emulsifying agents, binding agents, gases compressed to the liquid state, odorants, stabilizers, and the like.
- a wide variety of liquid and solid carriers can be used.
- Non-limiting examples of solid carriers include talc, bentonite, diatomaceous earth, pyrophyllite, fullers earth, gypsum, flours derived from cotton seeds and nut shells, and various natural and synthetic clays having a pH not exceeding about 9.5.
- Non-limiting examples of liquid carriers include water, organic solvents such as alcohols, ketones, amides and esters, mineral oils such as kerosene, light oils, and medium oils and vegetable oils such as cottonseed oil.
- herbicidal application is measured in terms of pounds of herbicide applied per acre.
- the compounds of this invention are effective herbicides when applied in herbicidal amounts, i.e., at rates between about 0.2 pounds and about 10 pounds per acre.
- All crop and weed species are planted individually in 3 inch plastic pots containing potting soil. Four seeds of each of corn, cotton, and snapbeans are seeded to a depth equal to the diameter of the seed. All other species are surface seeded and sprinkled with screened soil in an amount sufficient to cover the seeds. Immediately after planting, all pots are watered by sub-irrigation in greenhouse trays. Pots for the pre-emergence phase are seeded one day before treatment.
- Planting dates for the post-emergence phase are varied so that all the seedlings will reach the desired stage of developments simultaneously.
- the proper stage of seedling development for treatment in the post-emergence phase is as follows:
- Spray applications are made in a hood containing a movable belt and fixed spray nozzle.
- pre-emergence phase For passage through the spray hood, one pot of each species (pre-emergence phase) is placed on the forward half of a wooden flat and one pot of established plants (post-emergence phase) is placed on the rear half of the flat.
- Treatments are moved to the greenhouse after spraying. Watering during the observation period is applied only by subirrigation.
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Abstract
Metal salts and amine salts of 2-nitro-5-(halophenoxy)benzoic acids comprise a class of compounds that are highly effective pre- and post-emergence herbicides.
Description
This application is a continuation-in-part of copending application Ser. No. 194,479, filed Nov. 1, 1971, now U.S. Pat. No. 3,776,715 which is a division of application Ser. No. 819,412, filed Apr. 25, 1969, now U.S. Pat. No. 3,652,645.
1. Field of the Invention
This invention is concerned with certain phenoxybenzoic acid salts and their use as herbicides.
2. Description of the Prior Art
It has been proposed to use as herbicides 2-methoxybenzoic acids (U.S. Pat. No. 3,013,054) and 4-phenoxy-benzoic acids (French Pat. No. 1,502,538). It is the discovery of this invention, however, that benzoic acids having a phenoxy substituent in the 5-position are very effective herbicides. U.S. Pat. No. 3,475,427 discloses a position isomer of the acids disclosed herein. This isomeric acid and its salts are ineffective as herbicides.
This invention provides the method for controlling plant growth that comprises applying an herbicidal amount of an herbicidal compound having the formula: ##STR1## wherein X is halogen, n is 1 to 5, and M is alkali metal (Li, Na, K), alkaline earth metal (Ca, Mg, Ba, Sr), transition metal (e.g. Cu, Fe), ammonium, alkylammonium (C1 -C30), alkanolammonium (C1 -C3), alkyl (C1 -C30)dialkanol(C2 -C3)ammonium, dioxyalkylene(C2 -C3)alkyl(C1 -C30)-ammonium, dialkylammonium (C1 -C30), trialkylammonium (C1 -C30), alkoxyalkylammonium (C2 14 C6), dialkoxyalkyl ammonium (C3 -C6), aminoalkylammonium (C1 -C30), dialkylaminoalkylammonium (C3 -C8), alkenylammonium (C2 -C22), alkyl(C1 -C30)aminoalkyl(C2 -C6)ammonium, alkenyl(C2 -C30)aminoalkyl(C2 -C6)-ammonium, alkynyl(C3 -C12)ammonium, dialkenylammonium (C4 -C12), cycloalkylammonium (C3 -C6), alkyl(C1 -C30)ammoniumalkyl(C2 -C6)ammonium, benzylammonium, anilinium, substituted anilinium, guanidinium, or heterocyclicammonium (C4 -C6); and an herbicidal composition containing said compound.
The compounds of this invention are readily prepared by the Ullmann ether synthesis reaction between the alkali metal (Na, K) salt of a halophenol and a 5-halo (Cl, Br)-2-nitrobenzoic acid or an ester, amide, or salt thereof. The 5-halo-2-nitrobenzoic acid is readily prepared by nitrating a m-halotoluene, followed by oxidation of the methyl group by well-known procedures. Generally, the salts of this invention are prepared from the halophenoxybenzoic acid, using well known salt forming procedures.
The salts contemplated herein include metal salts, ammonium salts, and amine salts. The metal salts are the alkali metal salts (Li, Na, K); alkaline earth metal salts (Ca, Mg, Ba, etc.); and transition metal salts (Cu, Fe, etc.).
In addition to the salts of ammonia, the amine salts contemplated include salts of primary amines, secondary amines, tertiary amines, aryl amines, and heterocyclic amines. The primary amines can have 1-30 carbon atoms and can be saturated or unsaturated straight chain, branched chain, or cyclic. Non-limiting examples of primary amines are methylamine; ethylamine; n-propylamine; isopropylamine; n-butylamine; dodecylamine; triacontylamine; allylamine; 2-propynylamine; cyclohexylamine; propargylamine; isobutylamine; sec-butylamine; 2-ethylamine; cyclopropylmethylamine; t-butylamine; 1,1-dimethyl-2-propynylamine; 1,1-diethyl-2-propynlamine, tallow amine (E.G. Armeen I), 2,2-diethyl-2-dimethoxy ethylamine; 1-ethylnylcyclohexylamine and benzylamine.
The secondary amines can have 2-30 carbon atoms and can be saturated or unsaturated, straight chain, branched chain, or cyclic. Non-limiting examples of secondary amines are dimethylamine, diethylamine, dibutylamine, dioctylamine, ditetradecylamine, diallylamine, di-2-hexenylamine, dicyclohexylamine, methylethylamine, methyl cyclohexylamine, diisopropylamine, diisopentylamine, ethyl cyclohexylamine, (3-aminopropyl)alkenylamine wherein the alkenyl group has 16 to 18 carbon atoms; (3-aminopropyl)alkenylamine wherein the alkenyl group has 18, 20 and 22 carbon atoms; and dihydrogenated tallow amine (e.g. Armeen 2HT).
The tertiary amines can have 3-30 carbon atoms and can be saturated or unsaturated, straight chain, branched chain, or cyclic. Non-limiting examples of tertiary amines are trimethylamine, dimethyl ethylamine, triethylamine, tributylamine, trioctylamine, triallylamine, triisopentylamine, tricyclohexylamine, dimethyl octylamine, n-hexadecyldimethylamine (e.g. Armeen DM16D), n-octadecyldimethylamine (e.g. Armeen DM18D), methyl di-hydrogenated tallowamine (e.g. Armeen M2HT), and methyl di-cocoamine (e.g. Armeen M2C).
Non-limiting examples of arylamines are aniline; 2-chloroaniline; 3-chloroaniline; 4-chloroaniline; 2-methyl-4-chloroaniline; 2,4-dichloroaniline; 3,4-dichloroaniline; 2,6-dichloro-4-nitroaniline; m-trifluoromethylaniline; isopropylaniline; p-methoxyaniline; N-methoxymethyl-2,6-diethylaniline; α-naphthylaniline; N-sec-butyl-4-t-butyl-2,6-dinitroaniline; 3-amino-2,5-dichlorobenzoic acid; N,N-dipropyl α, α, α-trifluoro-2,6-dinitro-p-toluidine; 4-bromo-3-chloroaniline;4(4'-chlorophenoxy)aniline; N3, N3 -diethyl-2,4-dinitro-6-trifluoromethyl-m-phenylenediamine; p-dimethylaminoaniline; diphenylamine; p-bromoaniline; m-aminophenyl-t-butylcarbamate; o-phenylenediamine; m-phenylenediamine; 4-dimethylamino-3,5-dimethylphenol; 4-methylsulfonyl)-2,6-dinitro-N,N-dipropylaniline; 3,5-dinitro-N,N-dipropylsulfanilamide; N-sec-butyl-2,6-dinitroaniline; m-toluidine; p-toluidine; m-t-butylaniline; o-anisidine; p-anisidine; dimethylaniline; o-nitroaniline; p-nitroaniline; and 4,4'-oxydianiline.
Non-limiting examples of heterocyclic amines are 3-amino-1,2,4-triazole; 2-chloro-4-ethylamino-6-isopropylamino-s-triazine; pyridine; piperidine; piperazine; morpholine; 4,4'-dipyridyl; 8-hydroxyquinoline; 4-amino-6-t-butyl--(methylthio)-1,2,4-triazine-5(4H)-one; 6-ethoxy-1,2-dihydro-2,2,4-trimethylquinoline; indole; hexahydro-1H-azepine; 4-amino-5-chloro-2-phenyl-3(2H)-pyridazinone; pyrrole; imidazolidine; isoquinoline; 2,4-lutidine; 2-methyl-5-ethylpyridine; 2-dimethyl aminopyridine; α-picoline; β-picoline; γ-picoline; quinoline; and 4,4'-dipyridine.
Non-limiting examples of other salt-forming amino compounds contemplated are 2-chloroethyl dimethylamine; diethanolamine; quanidine; dodecylguanidine; 3-(4-chloro-phenyl)-1,1-dimethylurea; 3-(3,4-dichlorophenyl)-1,1-dimethylurea; Fenuron; Tandex β-alanine; methyl glycine; glycinamide; aminoacetonitrile; aminoethanthiol; aminoacetic acid; diethyl ethanolamine; diethylenetriamine; isopropanolamine; diisopropanolamine; triisopropanolamine; ethylenediamine; hexamethylenetetramine; hydrazine; phenothiazine; sulfanilic acid; tetraethylenepentamine; thiourea; urea; triethanolamine; triethylenetetramine; diethanol soyaamine (e.g. Ethomeen S-12) and didacaoxyethyene soyaamine (e.g. Ethomeen S-20).
The following example illustrates the preparation of a typical compound of this invention and demonstrates a method for product recovery.
A stirred solution of methyl 5-chloro-2-nitrobenzoate (17.0 g., 0.079 mole) and the potassium salt of 2,4,6-trichlorophenol (18.6 g., 0.079 mole) in dimethyl sulfoxide (100 ml.) was heated at 90° for 17 hours. The cooled reaction mixture was diluted with water (500 ml.) and then extracted with ether (3×100 ml.). The combined ether fractions were washed with 10% sodium hydroxide solution (2×30 ml.) and then with a saturated aqueous sodium chloride solution. The ether solution was dried (Na2 SO4) and the solvent evaporated to give a dark oil. Two crystallizations (petroleum ether) gave 1.91 g. of a pale yellow solid, m.p. 101°-103°.
Example 1
I.R. (numol): c=o 1723, c--o 1240, and 1260 cm-1
NMR (CDCl3): methyl 3.91 ppm (3H), quartet
6.96 ppm (1H, J=2.5 and 8 c.p.s.), doublet
7.05 ppm (1H, J=2.5 c.p.s.), broad singlet
7.05 ppm (2H), and doublet 8.01 ppm (1H, J=8 c.p.s.).
The ester of Example 1 was hydrolyzed to the corresponding acid and, using known salt-forming methods, salt compounds within the scope of this invention were prepared.
These compounds are identified below, wherein "A" represents a 2-nitro-5-(2',4'-dichlorophenoxy)benzoate group, "B" represents a 2-nitro-5-(2',4',6'-trichlorophenoxy) benzoate group, "C" represents a 2-nitro-5-(2',4'-dichloro-6'-fluorophenoxy)benzoate and "D" represents a 2-nitro-5-(2'-chloro-4'-fluorophenoxy)benzoate;
2. sodium B.
3. ethanolammonium B.
4. dimethylammonium B.
5. potassium A.
6. arachidyl (90%)-behenyl (10%) ammonium A.
7. arachidyl (90%)-behenyl(10%)aminopropylammonium A.
8. arachidyl (90%)-behenyl(10%)ammoniumpropylammonium bis-[A].
9. isobutylammonium A.
10. n-butylammonium A.
11. methoxypropylammonium A.
12. copper bis-[A].
13. 2,2-dimethoxyethylammonium A.
14. t-butylammonium A.
15. benzylammonium A.
16. allylammonium A.
17. diallyammonium A.
18. ethanolammonium A.
19. 3-dimethylaminopropylammonium A.
20. cyclohexylammonium A.
21. di-n-butylammonium A.
22. N,N-dimethyl-3-(4-methyl-3-cyclohexen-1-yl)butylammonium A.
23. 4-[3-(4-methyl-3-cyclohexen-1-yl)butyl]morpholium A.
24. N,N-dimethyl-3,3-dimethyl-2-norbornylethylammonium A.
29. calcium A.
30. n-propylammonium A.
31. 4(4'-aminophenoxy)anilinium A.
32. 4(4'-phenoxyammonium)anilinium A.
33. 2-propynylammonium A.
34. ammonium A.
35. diethanolammonium A.
36. triethanolammonium A.
37. methylammonium A.
38. trimethylammonium A.
39. isopropylammonium A.
40. sec-butylammonium A.
41. 2-dimethylaminopyridine A.
42. piperidine A.
43. morpholine A.
44. ethylammonium A.
45. diethylammonium A.
46. triethylammonium A.
47. p-methoxyanilinium A.
48. alkenyl(C16 -C18)aminopropylammonium A.
49. alkenyl(C18 -C20)aminopropylammonium A.
50. o-methoxyanilinium A.
51. m-methoxyanilinium A.
52. m-toluidine A.
53. p-toluidine A.
54. guanidine A.
55. anilinium A.
56. di(cyclohexyl)ammonium A.
57. 3,4-dichloroanilinium A.
58. m-chloroanilinium A.
59. p-chloroanilinium A.
60. isopropanolammonium A.
61. diisopropylammonium A.
62. 1,1-dimethyl-2-propynylammonium A.
63. 1,1-diethyl-2-propynylammonium A.
64. 1-ethynylcyclohexylammonium A.
65. n-dodecylaminea A. a=Armeen 12D
66. di(hydrogenated tallow)amineb A. b=Armeen 2HT
67. n-hexadecyldimethylaminec A. c=Armeen DM16D
68. n-octadecyldimethylamined A. d=Armeen DM18D
69. methyl di(hydrogenated tallow)aminee A. e=Armeen M2HT
70. methyl di-cocoaminef A. f=Armeen M2C
71. diethanol soyaamineg A. g=Ethomeen S-12
72. di(decaoxyethylene)soyaamineh A. h=Ethomeen S-20
73. 4,4'-dipyridinium A.
74. pyridinium A.
75. triisopropanolammonium A.
76. tallowaminei A. i=Armeen T
77. diethanolammonium C.
78. triethanolammonium C.
79. p-methoxyanilinium C.
80. ethanolammonium C.
81. sodium C.
82. ammonium C.
83. cyclohexylammonium C.
84. morpholine C.
85. o-methoxyanilinium C.
86. diethanolammonium B.
87. triethanolammonium B.
88. p-methoxyanilinium B.
89. cyclohexylammonium B.
90. morpholine B.
91. o-methoxyanilinium B.
92. diethanolammonium D.
93. triethanolammonium D.
94. p-methoxyanilinium D.
95. ethanolammonium D.
96. sodium D.
97. ammonium D.
98. cyclohexylammonium D.
99. morpholine D.
100. o-methoxyanilium D.
For comparison, a position isomer of the acids used to form the salts of this invention was prepared, as described in U.S. Pat. No. 3,475,427. Salts of this isomeric acid were prepared by known salt-forming methods. These compounds are:
(25) 2-nitro-3-(2',4'-dichlorophenoxy)benzoic acid.
(26) ethanolammonium 2-nitro-3-(2',4'-dichlorophenoxy)benzoate.
(27) n-propylammonium 2-nitro-3-(2',4'-dichlorophenoxy)benzoate.
(28) potassium 2-nitro-3-(2',4'-dichlorophenoxy)benzoate.
The compounds of this invention can be applied in various ways to achieve herbicidal action. They can be applied per se, as solids or in vaporized form, but are preferably applied as the toxic components in pesticidal compositions of the compound and a carrier. These compositions are preferably applied directly to the soil and incorporated therewith. The compositions can be applied, as granulars or dusts; as liquid sprays, or as gas-propelled sprays and can contain, in addition to a carrier, additives such as emulsifying agents, binding agents, gases compressed to the liquid state, odorants, stabilizers, and the like. A wide variety of liquid and solid carriers can be used. Non-limiting examples of solid carriers include talc, bentonite, diatomaceous earth, pyrophyllite, fullers earth, gypsum, flours derived from cotton seeds and nut shells, and various natural and synthetic clays having a pH not exceeding about 9.5. Non-limiting examples of liquid carriers include water, organic solvents such as alcohols, ketones, amides and esters, mineral oils such as kerosene, light oils, and medium oils and vegetable oils such as cottonseed oil.
In practice, herbicidal application is measured in terms of pounds of herbicide applied per acre. The compounds of this invention are effective herbicides when applied in herbicidal amounts, i.e., at rates between about 0.2 pounds and about 10 pounds per acre.
______________________________________
Crabgrass Digitaria sanguinalis
Yellow foxtail grass
Setaria glauca
Johnson grass Sorgum Halepense
Barnyard grass Echinochloa crus-galli
Amaranth pigweed Amaranthus retroflexus
Field bindweed Convoluvulus arvensis
Velvet leaf Abutilon theophrasti
Turnip Brassica sp.
Cotton Gossypium hirsutum var.
DPL smooth leaf
Corn Zea Mays var. Golden
Bantam
Bean Phaseolus vulgaris var.
Black Valentine
______________________________________
All crop and weed species are planted individually in 3 inch plastic pots containing potting soil. Four seeds of each of corn, cotton, and snapbeans are seeded to a depth equal to the diameter of the seed. All other species are surface seeded and sprinkled with screened soil in an amount sufficient to cover the seeds. Immediately after planting, all pots are watered by sub-irrigation in greenhouse trays. Pots for the pre-emergence phase are seeded one day before treatment.
Planting dates for the post-emergence phase are varied so that all the seedlings will reach the desired stage of developments simultaneously. The proper stage of seedling development for treatment in the post-emergence phase is as follows:
______________________________________
GRASSES: 2 inches in height
PIGWEED, BINDWEED, 1 or 2 true leaves visible
VELVET LEAF & TURNIPS:
above cotyledons
COTTON: first true leaf 1 inch in
length; expanded cotyledons
CORN: 3 inches-4 inches in height
BEANS: primary leaves expanded;
growing point at primary
leaf node.
______________________________________
Spray applications are made in a hood containing a movable belt and fixed spray nozzle. For passage through the spray hood, one pot of each species (pre-emergence phase) is placed on the forward half of a wooden flat and one pot of established plants (post-emergence phase) is placed on the rear half of the flat. Treatments are moved to the greenhouse after spraying. Watering during the observation period is applied only by subirrigation.
Compounds are screened initially at a rate of application equivalent to four to eight pounds per acre. Two weeks after treatment the pre- and post-emergence percent injury is visually rated. Subsequent testing can be carried out at 2,1 and 0.5 pounds per acre.
Herbicidal testing of the compounds of Examples 2 through 24 and 30 through 100 and the isomeric compounds showed the results set forth in Table I. The plants are tabulated using the following abbreviations:
TABLE I
__________________________________________________________________________
Compound
Dosage
Pre-/Post-Emergence
Ex. No.
Lbs./Acre
CG YF JG BG PW BW VL TP CT CN BN
__________________________________________________________________________
2 8 50/80 --/--
30/60
40/60
--/--
--/--
--/--
90/100
50/100
0/40
50/100
3 8 20/30 --/40
30/40
30/30
100/--
--/--
--/--
90/100
50/100
0/40
80/70
4 --/-- --/--
--/--
--/--
--/100
--/--
--/--
--/100
--/-- --/--
--/--
2 --/-- --/--
--/--
--/--
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__________________________________________________________________________
Crabgrass CG
Yellow foxtail grass
YF
Johnson grass
JG
Barnyard grass
BG
Pigweed PW
Bindweed BW
Velvet leaf
VL
Turnip TP
Cotton CT
Corn CN
Bean BN
Although the present invention has been described with preferred embodiments, it is to be understood that modifications and variations may be resorted to, without departing from the spirit and scope of this invention, as those skilled in the art will readily understand. Such modifications and variations are considered to be within the purview and scope of the appended claims.
Claims (8)
1. The method for controlling plant growth that comprises applying an herbicidal amount of an herbicidal compound having the formula: ##STR2## wherein X is halogen, n is 1 to 5, and M is alkali metal (Li, Na, K), .[.alkaline earth metal, a transition metal, ammonium, alkylammonium (C1 -C30), alkanolammonium (C1 -C3), alkyl (C1 -C30) dialkanol (C2 -C3) ammonium, dioxyalkylene (C2 -C3) alkyl (C1 -C30)ammonium, dialkylammonium (C1 -C30), trialkylammonium (C1 -C30), alkoxyalkylammonium (C2 -C6) dialkoxyalkylammonium (C3 -C6), aminoalkylammonium (C1 -C30), dialkylaminoalkylammonium (C3 -C8), alkenylammonium (C2 -C22), alkyl (C1 -C30 aminoalkyl (C2 -C6) ammonium, alkenyl (C2 -C30) aminoalkyl (C2 -C6) ammonium, alkynyl (C3 -C12) ammonium dialkenylammonium (C4 -C12), cycloalkylammonium (C3 -C6), alkyl (C1 -C30) ammonium alkyl (C2 -C6) ammonium, benzylammonium, anilinium, substituted anilinium, guanidinium or heterocyclicammonium (C.sub. 4 -C6)..]. .Iadd.alkylammonium (C1 -C4), or alkanolammonium (C1 -C3). .Iaddend. .[.
2. The method of claim 1, wherein said compound is butylammonium 2-nitro-5-(2',4'-dichlorophenoxy)benzoate..]. .[.3. The method of claim 1, wherein said compound is methoxypropylammonium 2-nitro-5-(2',4'-dichlorophenoxy) benzoate..]. .[.4. The method of claim 1, wherein said compound is cyclohexylammonium 2-nitro-5-(2',4'-dichlorophenoxy) benzoate..]. .[.5. The method of claim 1, wherein said compound is 2,2-dimethoxyethylammonium 2-nitro-5-(2',4'-dichlorophenoxy)benzoate..]. .[.6. The method of claim 1, wherein said compound is allylammonium 2-nitro-5-(2',4'-dichlorophenoxy)benzoate..]. .[.7. The method of claim 1, wherein said compound is arachidyl (90%) behenyl (10%) aminopropylammonium 2-nitro-5-(2',4'-dichlorophenoxy)benzoate..]. .[.8. The method of claim 1, wherein said compound is potassium
2-nitro-5-(2',4'-dichlorophenoxy)benzoate..]. 9. The method of claim 1, wherein said compund is ethanolammonium
2-nitro-5-(2',4',6'-trichlorophenoxy)benzoate. 10. The method of claim 1, wherein said compound is sodium
2-nitro-5-(2',4',6'-trichlorophenoxy)benzoate. 11. An herbicidal composition comprising a carrier for an herbicide and an herbicidal amount of an herbicidal compound having the formula: ##STR3## wherein X is halogen, n is 1 to 5, and M is alkali metal (Li, Na, K), .[.alkaline earth metal, a transition metal, ammonium, alkylammonium (C1 4 -C30), alkanolammonium (C1 -C3), alkyl (C1 -C30), dialkanol (C2 -C3) ammonium, dioxyalkylene (C2 -C3) alkyl (C1 -C30)ammonium, dialkylammonium (C1 -C30), trialkylammonium (C1 -C30), alkoxyalkylammonium (C2 -C6) dialkoxyalkylammonium (C3 -C6), aminoalkylammonium (C1 -C30), dialkylaminoalkylammonium (C3 -C8), alkenylammonium (C2 -C22), alkyl (C1 -C30) aminoalkyl (C2 -C6) ammonium, alkenyl (C2 -C30) aminoalkyl (C2 -C6) ammonium, alkynyl (C3 -C12)ammonium, dialkenylammonium (C4 -C12), cycloalkylammonium (C3 -C6), alkyl (C1 -C30) ammonium alkyl (C2 -C6) ammonium, benzylammonium, anilinium, substituted anilinium, guanidinium or heterocyclicammonium (C4 -C6)..]. .Iadd.alkylammonium (C1 -C4), or alkanolammonium (C1
-C3). .Iaddend. .[.12. The composition of claim 11, wherein said compound is butylammonium 2-nitro-5-(2',4'-dichlorophenoxy)benzoate..]. .[.13. The composition of claim 11, wherein said compound is methoxypropylammonium 2-nitro-5-(2',4'-dichlorophenoxy)benzoate..]. .[.14. The composition of claim 11, wherein said compound is cyclohexylammonium 2-nitro-5-(2',4'-dichlorophenoxy)benzoate.]. .[.15. The composition of claim 11, wherein said compound is 2,2-dimethoxyethylammonium 2-nitro-5-(2',4'-dichlorophenoxy)benzoate..]. .[.16. The composition of claim 11, wherein said compound is allylammonium 2-nitro-5-(2',4'-dichlorophenoxy)benzoate..]. .[.17. The composition of claim 11, wherein said compound is arachidyl (90% ) behenyl (10%) aminopropylammonium 2-nitro-5-(2',4'-dichlorophenoxy benzoate..]. .[.18. The composition of claim 11, wherein said compound is potassium
2-nitro-5-(2',4'-dichlorophenoxy)benzoate..]. 19. The composition of claim 11, wherein said compound is ethanolammonium
2-nitro-5-(2',4',6'-trichlorophenoxy)benzoate. 20. The composition of claim 11, wherein said compound is sodium 2-nitro-5-(2',4',6'-trichlorophenoxy)benzoate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/075,369 USRE32316E (en) | 1969-04-25 | 1979-09-14 | Substituted phenoxybenzoic acids and derivatives thereof |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US81941269A | 1969-04-25 | 1969-04-25 | |
| US06/075,369 USRE32316E (en) | 1969-04-25 | 1979-09-14 | Substituted phenoxybenzoic acids and derivatives thereof |
Related Parent Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US19447971A Continuation-In-Part | 1969-04-25 | 1971-11-01 | |
| US396630A Reissue US3929455A (en) | 1971-11-01 | 1973-09-12 | Herbicidal halophenoxy benzoic acid salts |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE32316E true USRE32316E (en) | 1986-12-30 |
Family
ID=26756757
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/075,369 Expired - Lifetime USRE32316E (en) | 1969-04-25 | 1979-09-14 | Substituted phenoxybenzoic acids and derivatives thereof |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USRE32316E (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4911754A (en) | 1987-07-16 | 1990-03-27 | American Cyanamid Company | Herbicidally active aryloxy saturated 5-membered benzo fused hetero-cyclic compounds |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3169849A (en) * | 1958-07-09 | 1965-02-16 | Upjohn Co | Method for controlling growth of undesired vegetation |
| US3423470A (en) * | 1965-12-09 | 1969-01-21 | Ciba Ltd | Pesticidal preparations and compounds |
| US3475427A (en) * | 1966-02-03 | 1969-10-28 | Smithkline Corp | Phenoxazines |
| DE2019821A1 (en) * | 1969-04-25 | 1970-11-12 | Mobil Oil Corp | Halophenoxybenzoic acids as herbicides and processes for their use |
| US3776961A (en) * | 1971-12-23 | 1973-12-04 | Oil Corp | 3-substituted 4-nitrophenyl halophenyl ethers |
| US3798276A (en) * | 1972-03-14 | 1974-03-19 | H Bayer | Herbicidal 4-trifluoromethyl-4'-nitrodiphenyl ethers |
-
1979
- 1979-09-14 US US06/075,369 patent/USRE32316E/en not_active Expired - Lifetime
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3169849A (en) * | 1958-07-09 | 1965-02-16 | Upjohn Co | Method for controlling growth of undesired vegetation |
| US3423470A (en) * | 1965-12-09 | 1969-01-21 | Ciba Ltd | Pesticidal preparations and compounds |
| US3475427A (en) * | 1966-02-03 | 1969-10-28 | Smithkline Corp | Phenoxazines |
| DE2019821A1 (en) * | 1969-04-25 | 1970-11-12 | Mobil Oil Corp | Halophenoxybenzoic acids as herbicides and processes for their use |
| US3776961A (en) * | 1971-12-23 | 1973-12-04 | Oil Corp | 3-substituted 4-nitrophenyl halophenyl ethers |
| US3798276A (en) * | 1972-03-14 | 1974-03-19 | H Bayer | Herbicidal 4-trifluoromethyl-4'-nitrodiphenyl ethers |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4911754A (en) | 1987-07-16 | 1990-03-27 | American Cyanamid Company | Herbicidally active aryloxy saturated 5-membered benzo fused hetero-cyclic compounds |
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