Synthesis of α‐Trifluoromethylated Ketones from Vinyl Triflates in the Absence of External Trifluoromethyl Sources

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  • Takuji Kawamoto
    Department of Applied Chemistry Yamaguchi University Ube Yamaguchi 755-8611 Japan
  • Rio Sasaki
    Department of Applied Chemistry Yamaguchi University Ube Yamaguchi 755-8611 Japan
  • Akio Kamimura
    Department of Applied Chemistry Yamaguchi University Ube Yamaguchi 755-8611 Japan

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<jats:title>Abstract</jats:title><jats:p>A novel method for the conversion of vinyl triflates into α‐trifluoromethylated ketones in the absence of external trifluoromethyl sources is described. This process accomplishes an efficient migration of the trifluoromethyl group of the triflate to the α‐position in the ketone through a radical process. The reaction proceeds by the addition of a trifluoromethyl radical to the vinyl triflate and subsequent fragmentation of the trifluoromethane sulfonyl radical. Based on this reaction, a one‐pot two‐step procedure for the trifluoromethylation of ketones was developed. The method presented herein also allows the transfer of perfluoroalkyl groups from vinyl perfluoroalkanesulfonates, which are readily accessible from alkynes and perfluoroalkanesulfonic acids.</jats:p>

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