A deeper insight into direct trifluoromethoxylation with trifluoromethyl triflate |
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Authors: | Olivier Marrec Thierry Billard Jean-Pierre Vors Bernard R. Langlois |
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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 |
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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. |
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Keywords: | Trifluoromethoxylation Trifluoromethoxide Trifluoromethyl triflate Trifluoromethyl trifluoromethanesulfonate Trifluoromethoxy-substitued compounds |
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