CN1021282C - 2-(1-(3-氯烯丙氧亚氨基)烷基)-5-烷硫基烷基-环己烷-1，3-二酮类除草剂 - Google Patents

2-(1-(3-氯烯丙氧亚氨基)烷基)-5-烷硫基烷基-环己烷-1，3-二酮类除草剂 Download PDF

Info

Publication number: CN1021282C
Authority: CN; China
Prior art keywords: compound; weight; propyl group; herbicidal combinations; trans
Prior art date: 1985-08-23
Legal status (The legal status 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 status listed.): Expired - Lifetime

Application number

CN90107624A

Other languages

English (en)

Chinese (zh)

Other versions

CN1051285A (zh

Inventor

塔塔奥·鲁欧

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Chevron USA Inc

Original Assignee

Chevron Research and Technology 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.)

1985-08-23

Filing date

1986-07-30

Publication date

1993-06-23

1986-07-30 Application filed by Chevron Research and Technology Co filed Critical Chevron Research and Technology Co

1991-05-15 Publication of CN1051285A publication Critical patent/CN1051285A/zh

1993-06-23 Application granted granted Critical

1993-06-23 Publication of CN1021282C publication Critical patent/CN1021282C/zh

2001-07-30 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000004009 herbicide Substances 0.000 title abstract description 13
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238000000034 method Methods 0.000 claims abstract description 27
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239000000203 mixture Substances 0.000 claims description 34
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
230000002363 herbicidal effect Effects 0.000 claims description 22
-1 2-methyl mercapto propyl group Chemical group 0.000 claims description 12
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
239000003960 organic solvent Substances 0.000 claims description 10
244000025670 Eleusine indica Species 0.000 claims description 8
235000014716 Eleusine indica Nutrition 0.000 claims description 8
235000015112 vegetable and seed oil Nutrition 0.000 claims description 8
239000008158 vegetable oil Substances 0.000 claims description 8
244000025254 Cannabis sativa Species 0.000 claims description 6
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239000003995 emulsifying agent Substances 0.000 claims description 4
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125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract description 18
231100000674 Phytotoxicity Toxicity 0.000 abstract description 15
238000002360 preparation method Methods 0.000 abstract description 11
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238000012360 testing method Methods 0.000 description 19
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QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 2
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JYCQQPHGFMYQCF-UHFFFAOYSA-N 4-tert-Octylphenol monoethoxylate Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCO)C=C1 JYCQQPHGFMYQCF-UHFFFAOYSA-N 0.000 description 1
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RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
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240000001505 Cyperus odoratus Species 0.000 description 1
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NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
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CSPPKDPQLUUTND-NBVRZTHBSA-N Sethoxydim Chemical compound CCO\N=C(/CCC)C1=C(O)CC(CC(C)SCC)CC1=O CSPPKDPQLUUTND-NBVRZTHBSA-N 0.000 description 1
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229910052783 alkali metal Inorganic materials 0.000 description 1
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229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
150000001350 alkyl halides Chemical class 0.000 description 1
125000006350 alkyl thio alkyl group Chemical group 0.000 description 1
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125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
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NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
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239000011591 potassium Substances 0.000 description 1
RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
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QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/02—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups
- C07C251/04—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C251/10—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton
- C07C251/16—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen
- A01N35/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical at least one of the bonds to hetero atoms is to nitrogen containing a carbon-to-nitrogen double bond
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/02—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups
- C07C251/24—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups bound to carbon atoms of six-membered aromatic rings

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CN90107624A 1985-08-23 1986-07-30 2-(1-(3-氯烯丙氧亚氨基)烷基)-5-烷硫基烷基-环己烷-1，3-二酮类除草剂 Expired - Lifetime CN1021282C (zh)

Applications Claiming Priority (5)

Application Number	Priority Date	Filing Date	Title
US76830185A	1985-08-23	1985-08-23
US768,301		1985-08-23
US79867085A	1985-11-15	1985-11-15
US798,670		1985-11-15
CN86105662A CN1011782B (zh)	1985-08-23	1986-07-30	2-[1-(3-氯烯丙氧基亚氨基)烷基]-5-烷硫基烷基-环己烷-1，3-二酮的制备方法

Related Parent Applications (1)

Application Number	Title	Priority Date	Filing Date
CN86105662A Division CN1011782B (zh)	1985-08-23	1986-07-30	2-[1-(3-氯烯丙氧基亚氨基)烷基]-5-烷硫基烷基-环己烷-1，3-二酮的制备方法

Publications (2)

Publication Number	Publication Date
CN1051285A CN1051285A (zh)	1991-05-15
CN1021282C true CN1021282C (zh)	1993-06-23

Family

ID=27118040

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
CN90107624A Expired - Lifetime CN1021282C (zh)	1985-08-23	1986-07-30	2-(1-(3-氯烯丙氧亚氨基)烷基)-5-烷硫基烷基-环己烷-1，3-二酮类除草剂
CN86105662A Expired CN1011782B (zh)	1985-08-23	1986-07-30	2-[1-(3-氯烯丙氧基亚氨基)烷基]-5-烷硫基烷基-环己烷-1，3-二酮的制备方法

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
CN86105662A Expired CN1011782B (zh)	1985-08-23	1986-07-30	2-[1-(3-氯烯丙氧基亚氨基)烷基]-5-烷硫基烷基-环己烷-1，3-二酮的制备方法

Country Status (14)

Country	Link
EP (1)	EP0236313A1 (fr)
KR (1)	KR920010518B1 (fr)
CN (2)	CN1021282C (fr)
AU (2)	AU586200B2 (fr)
BE (1)	BE903349A (fr)
CA (1)	CA1271644A (fr)
CH (2)	CH666890A5 (fr)
DE (1)	DE3627410A1 (fr)
FR (1)	FR2586416B1 (fr)
GB (2)	GB2188321B (fr)
NL (2)	NL193944C (fr)
NO (1)	NO162555C (fr)
SE (1)	SE458683B (fr)
WO (1)	WO1987001699A1 (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1987001699A1 (fr) *	1985-08-23	1987-03-26	Chevron Research Company	Herbicides de 2- ad1-(3-chloroallyloxyamino)alkylidene bd-5-alkylthioalkyle-cyclohexane-1,3-dione
ES2014493B3 (es) *	1986-04-24	1990-07-16	Ciba-Geigy Ag	Acil-ciclohexandionas y sus eteres de oximas con efecto herbicida y regulador del crecimiento de las plantas.
GB8722838D0 (en) *	1987-09-29	1987-11-04	Shell Int Research	Oximino ether compounds
JP2536075B2 (ja) *	1988-06-27	1996-09-18	住友化学工業株式会社	除草組成物
US5108488A (en) *	1989-07-21	1992-04-28	Valent U.S.A. Corporation	Synergistic herbicidal composition
US6300281B1 (en) *	2000-07-03	2001-10-09	Valent U.S.A. Corporation	Optically pure(−) clethodim, compositions and methods for controlling plant growth comprising the same
PL2321270T3 (pl)	2008-08-19	2016-09-30		Ulepszony sposób addycji tiolanów do alfa, beta-nienasyconych związków karbonylowych lub sulfonylowych
CN105418470B (zh) *	2015-11-17	2017-12-15	江苏长青农化股份有限公司	一种烯草酮的合成方法
CN106187841B (zh) *	2016-07-08	2018-01-30	山东润博生物科技有限公司	一种烯草酮的工业化制备方法
WO2020172219A1 (fr) *	2019-02-20	2020-08-27	Valent U.S.A. Llc	Compositions à base de cléthodime et leurs procédés d'utilisation
CN113024425B (zh) *	2019-12-24	2022-05-17	沈阳科创化学品有限公司	一种烯草酮的制备方法
CN112225682B (zh) *	2020-10-19	2022-02-25	中国科学院大连化学物理研究所	一种提高合成烯草酮反应速度的方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4440566A (en) *	1982-08-05	1984-04-03	Chevron Research Company	Herbicidal substituted 2-(1-(oxyamino)-alkylidene)-cyclohexane-1,3-diones
AU556148B2 (en) *	1982-01-29	1986-10-23	Ici Australia Limited	Cyclohexane -1,3- dione derivatives
WO1987001699A1 (fr) *	1985-08-23	1987-03-26	Chevron Research Company	Herbicides de 2- ad1-(3-chloroallyloxyamino)alkylidene bd-5-alkylthioalkyle-cyclohexane-1,3-dione

1985
- 1985-09-19 WO PCT/US1985/001786 patent/WO1987001699A1/fr not_active Ceased
- 1985-09-19 EP EP85904913A patent/EP0236313A1/fr active Pending
- 1985-09-19 KR KR1019860700645A patent/KR920010518B1/ko not_active Expired
- 1985-09-19 CH CH1974/87A patent/CH666890A5/de not_active IP Right Cessation
- 1985-09-19 AU AU49541/85A patent/AU586200B2/en not_active Expired
- 1985-09-19 NL NL8520309A patent/NL193944C/nl not_active IP Right Cessation
- 1985-09-19 GB GB8708127A patent/GB2188321B/en not_active Expired
- 1985-09-30 BE BE0/215661A patent/BE903349A/fr not_active IP Right Cessation
1986
- 1986-06-30 AU AU59380/86A patent/AU585999B2/en not_active Ceased
- 1986-07-22 NL NL8601900A patent/NL8601900A/nl not_active Application Discontinuation
- 1986-07-30 CN CN90107624A patent/CN1021282C/zh not_active Expired - Lifetime
- 1986-07-30 CN CN86105662A patent/CN1011782B/zh not_active Expired
- 1986-08-13 DE DE19863627410 patent/DE3627410A1/de not_active Withdrawn
- 1986-08-18 FR FR8611806A patent/FR2586416B1/fr not_active Expired
- 1986-08-19 CH CH3344/86A patent/CH667086A5/de not_active IP Right Cessation
- 1986-08-20 CA CA000516351A patent/CA1271644A/fr not_active Expired - Fee Related
- 1986-08-21 GB GB8620373A patent/GB2179352B/en not_active Expired
- 1986-09-15 SE SE8603868A patent/SE458683B/sv not_active IP Right Cessation
- 1986-09-18 NO NO86863733A patent/NO162555C/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
AU4954185A (en)	1987-04-07
AU586200B2 (en)	1989-07-06
CA1271644A (fr)	1990-07-17
CN1011782B (zh)	1991-02-27
NL8520309A (nl)	1985-09-19
CN86105662A (zh)	1987-04-08
DE3627410A1 (de)	1987-02-26
CH667086A5 (de)	1988-09-15
BE903349A (fr)	1986-04-01
CN1051285A (zh)	1991-05-15
EP0236313A1 (fr)	1987-09-16
GB2179352B (en)	1989-08-09
NO162555C (no)	1990-01-17
GB8708127D0 (en)	1987-05-13
KR920010518B1 (ko)	1992-12-04
GB2188321B (en)	1989-08-31
NO162555B (no)	1989-10-09
GB8620373D0 (en)	1986-10-01
CH666890A5 (de)	1988-08-31
SE8603868D0 (sv)	1986-09-15
FR2586416B1 (fr)	1989-06-02
WO1987001699A1 (fr)	1987-03-26
NO863733D0 (no)	1986-09-18
SE458683B (sv)	1989-04-24
FR2586416A1 (fr)	1987-02-27
AU5938086A (en)	1987-02-26
NO863733L (no)	1987-03-26
GB2188321A (en)	1987-09-30
GB2179352A (en)	1987-03-04
KR870700287A (ko)	1987-12-28
NL193944C (nl)	2001-03-02
SE8603868L (sv)	1987-03-20
NL8601900A (nl)	1987-03-16
AU585999B2 (en)	1989-06-29
NL193944B (nl)	2000-11-01

Legal Events

Date	Code	Title	Description
1991-04-24	C10	Entry into substantive examination
1991-04-24	SE01	Entry into force of request for substantive examination
1991-05-15	C06	Publication
1991-05-15	PB01	Publication
1993-06-23	C14	Grant of patent or utility model
1993-06-23	GR01	Patent grant
1994-10-19	C53	Correction of patent of invention or patent application
1994-10-19	COR	Change of bibliographic data	Free format text: CORRECT: APPLICANT; FROM: CHEVRON RESEARCH CO. TO: THOMEN COMPANY
1994-10-19	CP03	Change of name, title or address	Address after: Tokyo, Japan Applicant after: Thanks to the company Address before: california Applicant before: Chevron Research Co.
2002-03-20	C17	Cessation of patent right
2002-03-20	CX01	Expiry of patent term

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JPS6332078B2 (fr)	1988-06-28
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