DD144711A5 - Herbizide zusammensetzung und herbizides verfahren - Google Patents

Herbizide zusammensetzung und herbizides verfahren Download PDF

Info

Publication number: DD144711A5
Authority: DD; German Democratic Republic
Prior art keywords: trifluoroacetyl; phenyl; group; ethyl; glycinate
Prior art date: 1978-07-10

Application number

DD79214209A

Other languages

German (de)

English (en)

Inventor

John E Franz

Robert J Kaufman

Original Assignee

Monsanto Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1978-07-10

Filing date

1979-07-09

Publication date

1980-11-05

1979-07-09 Application filed by Monsanto Co filed Critical Monsanto Co

1980-11-05 Publication of DD144711A5 publication Critical patent/DD144711A5/de

Links

239000000203 mixture Substances 0.000 title claims description 36
230000002363 herbicidal effect Effects 0.000 title claims description 26
238000000034 method Methods 0.000 title claims description 8
-1 phosphonomethyl Chemical group 0.000 claims description 28
DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 claims description 23
150000001875 compounds Chemical class 0.000 claims description 20
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 20
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 19
125000000217 alkyl group Chemical group 0.000 claims description 11
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 8
125000004093 cyano group Chemical group *C#N 0.000 claims description 8
229910052736 halogen Inorganic materials 0.000 claims description 8
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
125000001424 substituent group Chemical group 0.000 claims description 7
239000000654 additive Substances 0.000 claims description 5
125000005843 halogen group Chemical group 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 5
230000000996 additive effect Effects 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
125000001624 naphthyl group Chemical group 0.000 claims description 4
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
239000001963 growth medium Substances 0.000 claims 1
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ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 33
239000000243 solution Substances 0.000 description 30
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239000003921 oil Substances 0.000 description 11
235000019198 oils Nutrition 0.000 description 11
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
238000004458 analytical method Methods 0.000 description 10
150000002148 esters Chemical class 0.000 description 9
239000000706 filtrate Substances 0.000 description 9
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239000004009 herbicide Substances 0.000 description 6
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238000006243 chemical reaction Methods 0.000 description 4
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IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
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239000000376 reactant Substances 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
239000011734 sodium Substances 0.000 description 3
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KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
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239000002253 acid Substances 0.000 description 2
XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
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150000001408 amides Chemical class 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
239000012736 aqueous medium Substances 0.000 description 2
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235000014113 dietary fatty acids Nutrition 0.000 description 2
239000012259 ether extract Substances 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
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239000011737 fluorine Substances 0.000 description 2
229910052731 fluorine Inorganic materials 0.000 description 2
230000002262 irrigation Effects 0.000 description 2
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229910052943 magnesium sulfate Inorganic materials 0.000 description 2
235000019341 magnesium sulphate Nutrition 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000002156 mixing Methods 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
239000006199 nebulizer Substances 0.000 description 2
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150000002989 phenols Chemical class 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
231100000208 phytotoxic Toxicity 0.000 description 2
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239000000843 powder Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000004576 sand Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
150000003871 sulfonates Chemical class 0.000 description 2
238000011282 treatment Methods 0.000 description 2
QAEDZJGFFMLHHQ-UHFFFAOYSA-N trifluoroacetic anhydride Chemical compound FC(F)(F)C(=O)OC(=O)C(F)(F)F QAEDZJGFFMLHHQ-UHFFFAOYSA-N 0.000 description 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
PFJVIOBMBDFBCJ-UHFFFAOYSA-N (1z)-1-diazobutane Chemical compound CCCC=[N+]=[N-] PFJVIOBMBDFBCJ-UHFFFAOYSA-N 0.000 description 1
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240000002245 Acer pensylvanicum Species 0.000 description 1
235000006760 Acer pensylvanicum Nutrition 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
240000001579 Cirsium arvense Species 0.000 description 1
235000005918 Cirsium arvense Nutrition 0.000 description 1
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244000058871 Echinochloa crus-galli Species 0.000 description 1
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244000248416 Fagopyrum cymosum Species 0.000 description 1
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244000068988 Glycine max Species 0.000 description 1
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244000286695 Melinis minutiflora var. inermis Species 0.000 description 1
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244000098338 Triticum aestivum Species 0.000 description 1
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125000003158 alcohol group Chemical group 0.000 description 1
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150000001412 amines Chemical class 0.000 description 1
239000000538 analytical sample Substances 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
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230000033228 biological regulation Effects 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
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JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 1
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PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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DIAIBWNEUYXDNL-UHFFFAOYSA-N n,n-dihexylhexan-1-amine Chemical compound CCCCCCN(CCCCCC)CCCCCC DIAIBWNEUYXDNL-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4087—Esters with arylalkanols
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4078—Esters with unsaturated acyclic alcohols
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4084—Esters with hydroxyaryl compounds

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

DD79214209A 1978-07-10 1979-07-09 Herbizide zusammensetzung und herbizides verfahren DD144711A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/922,920 US4218235A (en)	1978-07-10	1978-07-10	Ester derivatives of n-trifluoroacetyl-n-phosphonomethylglycine and the herbicidal use thereof

Publications (1)

Publication Number	Publication Date
DD144711A5 true DD144711A5 (de)	1980-11-05

Family

ID=25447789

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79214209A DD144711A5 (de)	1978-07-10	1979-07-09	Herbizide zusammensetzung und herbizides verfahren

Country Status (19)

Country	Link
US (1)	US4218235A (fr)
EP (1)	EP0007210B1 (fr)
JP (1)	JPS5513292A (fr)
AR (1)	AR226287A1 (fr)
AU (1)	AU520849B2 (fr)
BG (1)	BG29425A3 (fr)
BR (1)	BR7904359A (fr)
CA (1)	CA1131654A (fr)
CS (1)	CS208122B2 (fr)
DD (1)	DD144711A5 (fr)
DE (1)	DE2963001D1 (fr)
DK (1)	DK148325C (fr)
HU (1)	HU185007B (fr)
IL (1)	IL57750A (fr)
MX (1)	MX5593E (fr)
PH (1)	PH14396A (fr)
PL (1)	PL117606B1 (fr)
RO (2)	RO78802A (fr)
ZA (1)	ZA793416B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4444580A (en) *	1982-11-01	1984-04-24	Monsanto Company	N-Substituted N-(phosphonomethyl)aminoethanal derivatives as herbicides
US4444581A (en) *	1982-12-13	1984-04-24	Monsanto Company	Enamine derivatives of phosphonic acid esters as herbicides
US4569802A (en) *	1983-06-27	1986-02-11	Stauffer Chemical Company	Method for preparation of N-phosphonomethylglycine
US4654072A (en) *	1985-09-17	1987-03-31	Stauffer Chemical Company	Herbicidal phosphonomethyl amides

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3819353A (en) *	1968-05-24	1974-06-25	Du Pont	Plant growth regulant carbamoylphosphonates
US3853530A (en) *	1971-03-10	1974-12-10	Monsanto Co	Regulating plants with n-phosphonomethylglycine and derivatives thereof
PH16509A (en) *	1971-03-10	1983-11-08	Monsanto Co	N-phosphonomethylglycine phytotoxicant composition
US3799758A (en) *	1971-08-09	1974-03-26	Monsanto Co	N-phosphonomethyl-glycine phytotoxicant compositions
US3835000A (en) *	1972-12-21	1974-09-10	Monsanto Co	Electrolytic process for producing n-phosphonomethyl glycine
US3970695A (en) *	1975-05-23	1976-07-20	Monsanto Company	N-(perfluoroacyl)-N-phosphonomethyl glycine compounds, method of preparing same
US4108626A (en) *	1975-09-25	1978-08-22	E. I. Du Pont De Nemours And Company	Alkoxycarbonylphosphonic acid derivative brush control agents
MX3898E (es) *	1975-12-29	1981-09-10	Monsanto Co	Procedimiento mejorado para la preparacion de triesteres de n-fosfonometilglicina
US4053505A (en) *	1976-01-05	1977-10-11	Monsanto Company	Preparation of n-phosphonomethyl glycine
US4067719A (en) *	1976-12-13	1978-01-10	Monsanto Company	O-Aryl N-phosphonomethylglycinonitriles and the herbicidal use thereof

1978
- 1978-07-10 US US05/922,920 patent/US4218235A/en not_active Expired - Lifetime
1979
- 1979-07-06 EP EP79301306A patent/EP0007210B1/fr not_active Expired
- 1979-07-06 DE DE7979301306T patent/DE2963001D1/de not_active Expired
- 1979-07-09 IL IL57750A patent/IL57750A/xx unknown
- 1979-07-09 CA CA331,413A patent/CA1131654A/fr not_active Expired
- 1979-07-09 HU HU79MO1054A patent/HU185007B/hu unknown
- 1979-07-09 PL PL1979216974A patent/PL117606B1/pl unknown
- 1979-07-09 AU AU48773/79A patent/AU520849B2/en not_active Ceased
- 1979-07-09 PH PH22751A patent/PH14396A/en unknown
- 1979-07-09 BG BG7944252A patent/BG29425A3/xx unknown
- 1979-07-09 BR BR7904359A patent/BR7904359A/pt unknown
- 1979-07-09 RO RO7998093A patent/RO78802A/fr unknown
- 1979-07-09 DD DD79214209A patent/DD144711A5/de unknown
- 1979-07-09 DK DK287679A patent/DK148325C/da not_active IP Right Cessation
- 1979-07-09 CS CS794814A patent/CS208122B2/cs unknown
- 1979-07-09 ZA ZA793416A patent/ZA793416B/xx unknown
- 1979-07-09 JP JP8737779A patent/JPS5513292A/ja active Pending
- 1979-07-09 MX MX798167U patent/MX5593E/es unknown
- 1979-07-09 RO RO106307A patent/RO84199B/ro unknown
- 1979-07-16 AR AR277211A patent/AR226287A1/es active

Also Published As

Publication number	Publication date
HU185007B (en)	1984-11-28
EP0007210A3 (en)	1980-02-20
DE2963001D1 (en)	1982-07-22
CS208122B2 (en)	1981-08-31
DK148325C (da)	1985-11-04
IL57750A (en)	1983-02-23
PH14396A (en)	1981-06-25
ZA793416B (en)	1980-07-30
DK148325B (da)	1985-06-10
RO84199A (fr)	1984-06-21
DK287679A (da)	1980-01-11
RO78802A (fr)	1982-04-12
US4218235A (en)	1980-08-19
RO84199B (ro)	1984-08-30
MX5593E (es)	1983-11-03
PL216974A1 (fr)	1980-06-16
CA1131654A (fr)	1982-09-14
JPS5513292A (en)	1980-01-30
BG29425A3 (en)	1980-11-14
EP0007210A2 (fr)	1980-01-23
IL57750A0 (en)	1979-11-30
EP0007210B1 (fr)	1982-06-02
AU4877379A (en)	1980-01-17
AR226287A1 (es)	1982-06-30
PL117606B1 (en)	1981-08-31
BR7904359A (pt)	1980-04-08
AU520849B2 (en)	1982-03-04

Publication	Publication Date	Title
CH625393A5 (fr)	1981-09-30
EP0014684B1 (fr)	1982-05-19	Dérivés substitués en position 2 d'acides phénoxy-5 phénylphosphoniques, procédé pour leur préparation et leur utilisation comme herbicides
CH616662A5 (fr)	1980-04-15
DD256642A5 (de)	1988-05-18	Herbizide zusammensetzung
DE2406475A1 (de)	1974-08-29	2,4-dimethyltrifluormethansulfonanilide
EP0005782A1 (fr)	1979-12-12	Composés régulateurs de la croissance des plantes ainsi que les compositions contenant ces composés, leur application et leur préparation
DD213220A5 (de)	1984-09-05	Verfahren zur herstellung von n-phosphonomethylglycin
DD144712A5 (de)	1980-11-05	Herbizide zusammensetzung und herbizides verfahren
EP0075840B1 (fr)	1987-11-11	Phényléthers hétérocycliques, procédé pour leur préparation et herbicides les contenant
DE3012193A1 (de)	1980-10-09	Pyrazolylphosphorsaeureester, verfahren zu ihrer herstellung und sie enthaltende praeparate
DD144711A5 (de)	1980-11-05	Herbizide zusammensetzung und herbizides verfahren
EP0170842A1 (fr)	1986-02-12	Dérivés de N-benzylcyclopropanecarboxamide, procédé pour leur preperation et fongicides pour l'agriculture et l'horticulture
EP0158954A2 (fr)	1985-10-23	Dérivés de tétrahydroquinoline-1-yl carbonylimidazoles, leurs intermédiaires; leur procédé de préparation et herbicides ou fongicides pour l'agriculture ou l'horticulture
DD208293A5 (de)	1984-05-02	Zusammensetzung zur regulierung des pflanzenwachstums
EP0008624A1 (fr)	1980-03-19	Esters d'acides O-(pyridyloxy-phényl)-lactiques, leur procédé de préparation et leur utilisation comme herbicides et régulateurs de croissance de plantes
EP0050097B1 (fr)	1984-12-05	Dérivés de l'acide alpha-(pyridyl-2-oxy-phénoxy)-propionique, procédé pour leur préparation et leur utilisation comme herbicide et/ou régulateurs de croissance de plantes
DE2545569C3 (de)	1978-08-10	13-Dithiacyclopenten-2-ylidenmalonsäuredialkylester, Verfahren zu deren Herstellung und diese enthaltende fungizide Mittel
DD218268A5 (de)	1985-02-06	Herbizide zusammensetzung
EP0001641A1 (fr)	1979-05-02	Ester methoxyethylique de l'acide 2(2'-Nitro-5-(2"-chloro-4" trifluoromethylphenoxy)-phenoxy) propionique, une composition contenant cet ester comme substance active, et son utilisation comme herbicide.
EP0071572A2 (fr)	1983-02-09	Dérivés de l'acide nitro-2 pyridyloxy-4 ou -5 phosphonique, leur procédé de préparation, leur utilisation comme herbicides et/ou régulateurs de la croissance des plantes et/ou microbicides, ainsi que les intermédiaires utilisés pour leur préparation, leur procédé de préparation et leur utilisation comme herbicides
EP0066771B1 (fr)	1984-10-03	1-Iodo-1-propyn-3-ols, procédé pour leur préparation et leur utilisation comme agent de protection des plantes
DE2519085C3 (de)	1978-05-18	Substituierte Benzolmethanolverbindungen und diese enthaltende herbizide Mittel
DD144714A5 (de)	1980-11-05	Herbizides gemisch
DE2644486C2 (de)	1984-11-22	Substituierte Phenoxybenzoesäureanhydride, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbicide
DE2921567A1 (de)	1980-01-24	Ungesaettigte pyridyloxyphenoxyderivate, verfahren zur herstellung derselben und herbizide mittel mit einem gehalt derselben