首页 | 本学科首页   官方微博 | 高级检索  
     


A deeper insight into direct trifluoromethoxylation with trifluoromethyl triflate
Authors:Olivier Marrec  Thierry Billard  Jean-Pierre Vors  Bernard R. Langlois
Affiliation:a ICBMS, Institut de Chimie et Biochimie Moléculaires et Supramoléculaires, Equipe SERCOF, 43 boulevard du 11 novembre 1918, Villeurbanne, F-69622, France
b CNRS, UMR5246, Villeurbanne, F-69622, France
c Université de Lyon, Lyon, F-69622, France
d Université Lyon 1, Lyon, F-69622, France
e INSA-Lyon, Villeurbanne, F-69622, France
f CPE Lyon, Villeurbanne, F-69616, France
g Bayer CropScience AG, Product Technology, Process Research, Building 6550, Alfred-Nobel-Str. 50, 40789 Monheim am Rhein, Germany
Abstract:Commercially available fluorides (silver fluoride and n-tetrabutylammonium triphenyldifluorosilicate), combined with TFMT, allow a simple generation, in situ, of silver and n-tetrabutylammonium trifluoromethoxides which were able to react with electrophilic substrates. Silver trifluoromethoxide, which is usually more efficient than n-tetrabutylammonium trifluoromethoxide, converts, under mild conditions, primary aliphatic bromides and iodides, as well as primary and secondary benzylic or allylic bromides to the corresponding trifluoromethoxylated compounds. Several trifluoromethyl ethers, which could be valuable building-blocks, were prepared in such a way.
Keywords:Trifluoromethoxylation   Trifluoromethoxide   Trifluoromethyl triflate   Trifluoromethyl trifluoromethanesulfonate   Trifluoromethoxy-substitued compounds
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号