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Title:
ビニルフルオロアルカンスルホナート化合物の製造方法
Document Type and Number:
Japanese Patent JP7017229
Kind Code:
B2
Abstract:
To provide a method for producing 3,3,3-trifluoromethyl-1-arylalken-1-yltrifluoromethane sulfonate and an analog thereof, as a building block useful for development of pharmaceuticals, agrochemicals and the like, at a low cost and without using transition metal catalysts.SOLUTION: The present invention provides a method for producing a vinyl fluoroalkane sulfonate compound represented by formula (III), including reacting an alkyne compound such as 1-phenyl-1-hexyne with a fluoroalkane sulfonic acid anhydride in the presence of a polycyclic tertiary amine and acetonitrile [in the formula, each R independently represents a hydrogen atom, a C1-C10 alkyl group or the like: Ris a C1-C10 fluoroalkyl group; and the wavy line represents either a trans or cis configuration, or a mixture thereof).SELECTED DRAWING: None

Inventors:
Takuji Kawamoto
Junya Mitsui
Akio Uemura
Application Number:
JP2017217052A
Publication Date:
February 08, 2022
Filing Date:
November 10, 2017
Export Citation:
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Assignee:
Yamaguchi University
International Classes:
C07C303/26; C07C309/65
Other References:
Tomita, Ren 他,Photoredox-Catalyzed Stereoselective Conversion of Alkynes into Tetrasubstituted Trifluoromethylated Alkenes,Angewandte Chemie, International Edition ,2015年,54(44),12923-12927
Wang, Xi 他,Regio- and Stereoselective Radical Perfluoroalkyltriflation of Alkynes Using Phenyl(perfluoroalkyl)iodonium Triflates,Organic Letters,2017年05月,19(11),2977-2980
Nenajdenko, Valentine G. 他,Synthesis of β-dimethylsulfonium- and β-methylthio-substituted vinyl triflates by reaction of acetylenes with dimethyl sulfide ditriflate,Synthesis,1997年,(3),351-355
Attorney, Agent or Firm:
Hiroki Masaki
Seiji Ozawa
Yusaku Tokai
Kazuhiro Matsuda
Horiuchi Makoto
Masako Yamauchi
Shuichi Sonomoto
Akihiro Yamamura
Satoshi Morikawa
Hiroyuki Tomita