HU184202B - Selective herbicide composition containing 3-/methoxy-carbonyl-mino/-phenyl ester of n-ethyl-carbamidic acid and process for preparing 3-/methoxy-carbonyl-amino/-phenyl ester of n-ethyl-n-phenyl-carbamidic acid - Google Patents

Selective herbicide composition containing 3-/methoxy-carbonyl-mino/-phenyl ester of n-ethyl-carbamidic acid and process for preparing 3-/methoxy-carbonyl-amino/-phenyl ester of n-ethyl-n-phenyl-carbamidic acid Download PDF

Info

Publication number: HU184202B
Authority: HU; Hungary
Prior art keywords: ethyl; carbonyl; methoxy; phenyl; phenyl ester
Prior art date: 1978-05-02

Application number

HU79SCHE677A

Other languages

English (en)

Hungarian (hu)

Inventor

Friedrich Arndt

Gerhard Boroschewski

Original Assignee

Schering Ag

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.)

1978-05-02

Filing date

1979-04-27

Publication date

1984-07-30

1979-04-27 Application filed by Schering Ag filed Critical Schering Ag

1984-07-30 Publication of HU184202B publication Critical patent/HU184202B/hu

Links

239000002253 acid Substances 0.000 title claims description 4
230000002363 herbicidal effect Effects 0.000 title abstract description 4
238000004519 manufacturing process Methods 0.000 title abstract 2
239000004009 herbicide Substances 0.000 title description 2
239000000203 mixture Substances 0.000 title description 2
125000006626 methoxycarbonylamino group Chemical group 0.000 title 1
TWWODOWIDRHPDM-UHFFFAOYSA-N [3-(methoxycarbonylamino)phenyl] n-ethyl-n-phenylcarbamate Chemical compound C=1C=CC=CC=1N(CC)C(=O)OC1=CC=CC(NC(=O)OC)=C1 TWWODOWIDRHPDM-UHFFFAOYSA-N 0.000 claims description 3
150000001412 amines Chemical class 0.000 claims description 3
238000000034 method Methods 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
150000002148 esters Chemical class 0.000 claims description 2
XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 claims description 2
PWXJULSLLONQHY-UHFFFAOYSA-N phenylcarbamic acid Chemical class OC(=O)NC1=CC=CC=C1 PWXJULSLLONQHY-UHFFFAOYSA-N 0.000 abstract description 3
150000001875 compounds Chemical class 0.000 abstract description 2
235000003276 Apios tuberosa Nutrition 0.000 abstract 1
244000105624 Arachis hypogaea Species 0.000 abstract 1
235000010777 Arachis hypogaea Nutrition 0.000 abstract 1
235000010744 Arachis villosulicarpa Nutrition 0.000 abstract 1
229920000742 Cotton Polymers 0.000 abstract 1
241000219146 Gossypium Species 0.000 abstract 1
240000007594 Oryza sativa Species 0.000 abstract 1
235000007164 Oryza sativa Nutrition 0.000 abstract 1
235000009566 rice Nutrition 0.000 abstract 1
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
XIZDNZVKQNBGGR-UHFFFAOYSA-N (3-aminophenyl) n-ethyl-n-phenylcarbamate Chemical compound C=1C=CC=CC=1N(CC)C(=O)OC1=CC=CC(N)=C1 XIZDNZVKQNBGGR-UHFFFAOYSA-N 0.000 description 2
UXJXCTURSMEGTA-UHFFFAOYSA-N (3-nitrophenyl) n-ethyl-n-phenylcarbamate Chemical compound C=1C=CC=CC=1N(CC)C(=O)OC1=CC=CC([N+]([O-])=O)=C1 UXJXCTURSMEGTA-UHFFFAOYSA-N 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
239000007868 Raney catalyst Substances 0.000 description 2
229910000564 Raney nickel Inorganic materials 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 2
-1 chloroformic acid 3- (methoxycarbonylamino) phenyl esters Chemical class 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
238000003756 stirring Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical class NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 1
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
IMNFDUFMRHMDMM-UHFFFAOYSA-N anhydrous n-heptane Natural products CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
AAPAVYWERMFERN-UHFFFAOYSA-N ethyl(phenyl)carbamic acid Chemical compound CCN(C(O)=O)C1=CC=CC=C1 AAPAVYWERMFERN-UHFFFAOYSA-N 0.000 description 1
238000001914 filtration Methods 0.000 description 1
SIZKDIQMNFWPBD-UHFFFAOYSA-N hydroxy(phenyl)carbamic acid Chemical class OC(=O)N(O)C1=CC=CC=C1 SIZKDIQMNFWPBD-UHFFFAOYSA-N 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
239000000395 magnesium oxide Substances 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
150000007530 organic bases Chemical group 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1

Classifications

- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

HU79SCHE677A 1978-05-02 1979-04-27 Selective herbicide composition containing 3-/methoxy-carbonyl-mino/-phenyl ester of n-ethyl-carbamidic acid and process for preparing 3-/methoxy-carbonyl-amino/-phenyl ester of n-ethyl-n-phenyl-carbamidic acid HU184202B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2819748A DE2819748C2 (de)	1978-05-02	1978-05-02	N-Äthylcarbanilsäure-(3-methoxycarbonylamino)-phenylester, Verfahren zur Herstellung dieser Verbindung sowie diese enthaltendes selektives herbizides Mittel

Publications (1)

Publication Number	Publication Date
HU184202B true HU184202B (en)	1984-07-30

Family

ID=6038754

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
HU79SCHE677A HU184202B (en)	1978-05-02	1979-04-27	Selective herbicide composition containing 3-/methoxy-carbonyl-mino/-phenyl ester of n-ethyl-carbamidic acid and process for preparing 3-/methoxy-carbonyl-amino/-phenyl ester of n-ethyl-n-phenyl-carbamidic acid

Country Status (31)

Country	Link
JP (1)	JPS54144338A (fr)
AR (1)	AR222653A1 (fr)
AT (1)	AT365895B (fr)
AU (1)	AU522366B2 (fr)
BE (1)	BE875991A (fr)
BR (1)	BR7902627A (fr)
CA (1)	CA1108639A (fr)
CH (1)	CH639946A5 (fr)
CS (1)	CS207787B2 (fr)
DD (1)	DD143200A5 (fr)
DE (1)	DE2819748C2 (fr)
EG (1)	EG13834A (fr)
ES (1)	ES478923A1 (fr)
FI (1)	FI790909A7 (fr)
FR (1)	FR2424905A1 (fr)
GB (1)	GB2020283B (fr)
GR (1)	GR73571B (fr)
HU (1)	HU184202B (fr)
IL (1)	IL57073A (fr)
IN (1)	IN150828B (fr)
IT (1)	IT1166730B (fr)
MX (1)	MX5787E (fr)
NL (1)	NL7901680A (fr)
PH (1)	PH14259A (fr)
PL (1)	PL116642B1 (fr)
PT (1)	PT69398A (fr)
RO (3)	RO80177A (fr)
SE (1)	SE7902441L (fr)
SU (1)	SU852167A3 (fr)
TR (1)	TR20603A (fr)
YU (1)	YU40364B (fr)

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1567151C3 (de) *	1965-04-09	1974-02-21	Schering Ag, 1000 Berlin Und 4619 Bergkamen	Diurethane, Verfahren zur Herstellung dieser Verbindungen sowie diese enthaltende herbizide Mittel
US3535101A (en) *	1966-09-07	1970-10-20	Schering Ag	Herbicide and algicide means
US3901936A (en) *	1966-10-15	1975-08-26	Schering Ag	Process for the preparation of n-carbamoyloxyphenyl carbamates
JPS5140073A (fr) *	1974-06-28	1976-04-03	Siemens Ag
DE2557552C2 (de) *	1975-12-18	1984-12-20	Schering AG, 1000 Berlin und 4709 Bergkamen	Diurethane und herbizide Mittel, enthaltend diese Verbindungen als Wirkstoffe

1978
- 1978-05-02 DE DE2819748A patent/DE2819748C2/de not_active Expired
1979
- 1979-03-02 NL NL7901680A patent/NL7901680A/xx not_active Application Discontinuation
- 1979-03-16 FI FI790909A patent/FI790909A7/fi not_active Application Discontinuation
- 1979-03-19 YU YU667/79A patent/YU40364B/xx unknown
- 1979-03-19 SE SE7902441A patent/SE7902441L/ unknown
- 1979-03-23 ES ES478923A patent/ES478923A1/es not_active Expired
- 1979-03-27 PT PT69398A patent/PT69398A/pt unknown
- 1979-03-29 IN IN208/DEL/79A patent/IN150828B/en unknown
- 1979-04-06 IT IT21636/79A patent/IT1166730B/it active
- 1979-04-07 GR GR58833A patent/GR73571B/el unknown
- 1979-04-15 IL IL7957073A patent/IL57073A/xx unknown
- 1979-04-18 AR AR276229A patent/AR222653A1/es active
- 1979-04-20 CS CS792753A patent/CS207787B2/cs unknown
- 1979-04-23 GB GB7914092A patent/GB2020283B/en not_active Expired
- 1979-04-25 DD DD79212488A patent/DD143200A5/de unknown
- 1979-04-25 CA CA326,275A patent/CA1108639A/fr not_active Expired
- 1979-04-26 MX MX797937U patent/MX5787E/es unknown
- 1979-04-27 HU HU79SCHE677A patent/HU184202B/hu unknown
- 1979-04-27 SU SU792757223A patent/SU852167A3/ru active
- 1979-04-30 PH PH22442A patent/PH14259A/en unknown
- 1979-04-30 TR TR20603A patent/TR20603A/xx unknown
- 1979-04-30 CH CH405879A patent/CH639946A5/de not_active IP Right Cessation
- 1979-04-30 AT AT0323279A patent/AT365895B/de not_active IP Right Cessation
- 1979-04-30 BR BR7902627A patent/BR7902627A/pt unknown
- 1979-04-30 RO RO79104234A patent/RO80177A/fr unknown
- 1979-04-30 PL PL1979215274A patent/PL116642B1/pl unknown
- 1979-04-30 RO RO7987405A patent/RO78022A/fr unknown
- 1979-05-01 AU AU46578/79A patent/AU522366B2/en not_active Ceased
- 1979-05-01 JP JP5256679A patent/JPS54144338A/ja active Pending
- 1979-05-02 EG EG254/79A patent/EG13834A/xx active
- 1979-05-02 FR FR7911009A patent/FR2424905A1/fr active Granted
- 1979-05-02 BE BE0/194952A patent/BE875991A/fr not_active IP Right Cessation
- 1979-05-30 RO RO79104223A patent/RO80176A/fr unknown

Also Published As

Publication number	Publication date
DD143200A5 (de)	1980-08-13
BR7902627A (pt)	1979-11-27
TR20603A (tr)	1982-01-01
SE7902441L (sv)	1979-11-03
FR2424905A1 (fr)	1979-11-30
RO78022A (fr)	1982-02-01
RO80177A (fr)	1982-10-26
SU852167A3 (ru)	1981-07-30
EG13834A (en)	1982-06-30
CA1108639A (fr)	1981-09-08
RO80176A (fr)	1982-10-26
MX5787E (es)	1984-07-11
PH14259A (en)	1981-04-23
IN150828B (fr)	1982-12-25
PT69398A (de)	1979-04-01
YU40364B (en)	1985-12-31
ATA323279A (de)	1981-07-15
IT1166730B (it)	1987-05-06
IL57073A (en)	1983-07-31
AU4657879A (en)	1979-11-29
GR73571B (fr)	1984-03-19
GB2020283A (en)	1979-11-14
BE875991A (fr)	1979-11-05
AR222653A1 (es)	1981-06-15
PL215274A1 (fr)	1980-02-11
CS207787B2 (en)	1981-08-31
ES478923A1 (es)	1980-01-01
FR2424905B1 (fr)	1984-07-20
IT7921636A0 (it)	1979-04-06
PL116642B1 (en)	1981-06-30
FI790909A7 (fi)	1979-11-03
AU522366B2 (en)	1982-06-03
JPS54144338A (en)	1979-11-10
DE2819748C2 (de)	1986-07-31
DE2819748A1 (de)	1979-11-15
YU66779A (en)	1983-02-28
GB2020283B (en)	1982-10-27
CH639946A5 (de)	1983-12-15
NL7901680A (nl)	1979-11-06
AT365895B (de)	1982-02-25
IL57073A0 (en)	1979-07-25

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JPH045026B2 (fr)	1992-01-30
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