Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1313554 | Journal of Fluorine Chemistry | 2016 | 8 Pages |
Abstract
•An efficient method for the synthesis of fluorovinyl pyrazolyl (thio)ethers is reported.•The reaction of gem-difluoroalkenes with pyrazolin-5-ones (thiones) proceeds efficiently under mild conditions.•The addition of potassium tert-butoxide is essential for efficient conversion.
A mild and efficient method for the preparation of fluorovinyl pyrazolyl ethers and thioethers by the reaction of gem-difluoroalkenes having aryl substituents with pyrazolin-5-ones and pyrazolin-5-thiones, respectively, in the presence of t-BuOK is described.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Tao Huang, Xianghu Zhao, Xinfei Ji, Wei Wu, Song Cao,