[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

GB2005269A - Preparation of 3-phenoxybenzyl 3(2,2-dihalovinyl)-2,2- dimethylcyclopropanecarboxylate - Google Patents

Preparation of 3-phenoxybenzyl 3(2,2-dihalovinyl)-2,2- dimethylcyclopropanecarboxylate

Info

Publication number
GB2005269A
GB2005269A GB7838708A GB7838708A GB2005269A GB 2005269 A GB2005269 A GB 2005269A GB 7838708 A GB7838708 A GB 7838708A GB 7838708 A GB7838708 A GB 7838708A GB 2005269 A GB2005269 A GB 2005269A
Authority
GB
United Kingdom
Prior art keywords
dihalovinyl
dimethylcyclopropanecarboxylate
phenoxybenzyl
preparation
lower alkyl
Prior art date
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.)
Granted
Application number
GB7838708A
Other versions
GB2005269B (en
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.)
FMC Corp
Original Assignee
FMC Corp
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.)
Filing date
Publication date
Application filed by FMC Corp filed Critical FMC Corp
Publication of GB2005269A publication Critical patent/GB2005269A/en
Application granted granted Critical
Publication of GB2005269B publication Critical patent/GB2005269B/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
    • C07C69/743—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring of acids with a three-membered ring and with unsaturation outside the ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/02—Systems containing only non-condensed rings with a three-membered ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

The insecticide, 3-phenoxybenzyl 3-(2,2-dihalovinyl)-2,2- dimethylcyclopropanecarboxylate, is produced in high yield by the alcoholysis of a lower alkyl 3-(2,2- dihalovinyl)-2,2- dimethylcyclopropanecarboxylate with 3-phenoxybenzyl alcohol in the presence of a catalytic quantity of lower alkyl titanium alkoxide.
GB7838708A 1977-10-03 1978-09-29 Process to 3-phenoxybenzyl 3-(2,2-dihalovinyl)-2,2-dimethylcyclopropanecarboxylate Expired GB2005269B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US83905177A 1977-10-03 1977-10-03

Publications (2)

Publication Number Publication Date
GB2005269A true GB2005269A (en) 1979-04-19
GB2005269B GB2005269B (en) 1982-03-10

Family

ID=25278739

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7838708A Expired GB2005269B (en) 1977-10-03 1978-09-29 Process to 3-phenoxybenzyl 3-(2,2-dihalovinyl)-2,2-dimethylcyclopropanecarboxylate

Country Status (6)

Country Link
JP (1) JPS5459265A (en)
BR (1) BR7806542A (en)
CA (1) CA1123855A (en)
GB (1) GB2005269B (en)
GT (1) GT197854452A (en)
MX (1) MX5105E (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5154841A (en) * 1988-12-21 1992-10-13 The Procter & Gamble Company Process for preparing substituted imidazoline fabric conditioning compounds
EP1061065A2 (en) * 1999-06-16 2000-12-20 Sumitomo Chemical Company, Limited Methods for producing cyclopropane carboxylates
US6531626B1 (en) * 1998-10-08 2003-03-11 Sumitomo Chemical Company, Limited Method for producing cyclopropanecarboxylates

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8084559B2 (en) 2005-01-28 2011-12-27 Sumitomo Chemical Company, Limited Transition metal complex, process for producing said transition metal complex, substituent-carrying fluorene compound, process for producing said fluorene compound, catalyst component for olefin polymerization, catalyst for olefin polymerization, and process for producing olefin polymer

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5154841A (en) * 1988-12-21 1992-10-13 The Procter & Gamble Company Process for preparing substituted imidazoline fabric conditioning compounds
US6531626B1 (en) * 1998-10-08 2003-03-11 Sumitomo Chemical Company, Limited Method for producing cyclopropanecarboxylates
EP1061065A2 (en) * 1999-06-16 2000-12-20 Sumitomo Chemical Company, Limited Methods for producing cyclopropane carboxylates
EP1061065A3 (en) * 1999-06-16 2001-11-28 Sumitomo Chemical Company, Limited Methods for producing cyclopropane carboxylates
US6441220B1 (en) * 1999-06-16 2002-08-27 Sumitomo Chemical Company, Limited Methods for producing cyclopropane carboxylates
KR100679902B1 (en) * 1999-06-16 2007-02-07 스미또모 가가꾸 가부시끼가이샤 Methods for producing cyclopropane carboxylates

Also Published As

Publication number Publication date
JPS5459265A (en) 1979-05-12
CA1123855A (en) 1982-05-18
JPS5549065B2 (en) 1980-12-10
BR7806542A (en) 1979-05-02
GT197854452A (en) 1980-03-25
MX5105E (en) 1983-03-16
GB2005269B (en) 1982-03-10

Similar Documents

Publication Publication Date Title
IL54149A (en) Fluoro-3-phenoxybenzyl alcohol and its esters with 2,2-dimethyl-3-(2,2-disubstituted vinyl)cyclopropane carboxylic and alpha-isopropylphenylacetic acids,their preparation and the use of the esters as insecticides and acaricides
PL218526A1 (en)
USD258311S (en) Specimen collection device
GB2000126B (en) Preparation of 1,4-diols by hydrolysis-hydrogenation of 2-alkoxytetrahydrofurans
GB2005269A (en) Preparation of 3-phenoxybenzyl 3(2,2-dihalovinyl)-2,2- dimethylcyclopropanecarboxylate
JPS54128556A (en) Novel pentafluorobenzyloxycarbonyl derivative* its preparation and its use as insecticide and miticide
JPS5424827A (en) Preparation of carbonate ester
DE2961651D1 (en) Process for the preparation of cyclopropane derivatives, intermediates in the synthesis of pyrethroid insecticides
NZ184241A (en) A process for the preparation of certain cyano-substituted ester -cyano-3-phenoxybenzyl 3-(2,2-dichl-orovinyl)-2,2-dimethyl-cyclopropane carboxylate insecticidal composition
GB2016459B (en) Process for the preparation of an optically active -cyano alcohol ether
AU5337279A (en) Insecticidal substituted cyclopropane and cyclobutane derivatives
JPS53147003A (en) Preparation of beta,gamma-unsaturated compounds
PT70223A (en) Process for the preparation of substituted bromostyryl-cyclopropanecarboxylates with insecticidal and acaricidal activity
DK649587A (en) PROCEDURE FOR PREPARING A POLYMER
DE3164589D1 (en) Methyl esters of 2,2-dimethyl cyclopropane-1,3-dicarboxylic acid, their preparation and intermediales obtained
JPS53105461A (en) Preparation of 2,2-dimethyl-3(2-halo-1-propenyl)cyclopropane-1-carboxylic acid ester
JPS53127427A (en) Preparation of 3,4-dichlorophenol
JPS53103458A (en) Isomerization of cyanonorbornene
JPS54109910A (en) Preparation of unsaturated ester
JPS53103457A (en) Preparation of exo-cyanonorbornene
JPS53132541A (en) Optically active 2-alkyl-4-isopropenyl cyclohexanone and its preparation
GB2021104A (en) Preparation of a bicyclohexene
JPS5428282A (en) Formation of transparent gel of alcohols
JPS5359032A (en) Repellents to termite for soil application
JPS52153910A (en) Preparation of dimethylaminoethylmethacrylate

Legal Events

Date Code Title Description
PE20 Patent expired after termination of 20 years

Effective date: 19980928