Department of Applied Chemistry, Yamaguchi University, Ube, Yamaguchi, 755-8611, Japan.
Angew Chem Int Ed Engl. 2017 Jan 24;56(5):1342-1345. doi: 10.1002/anie.201608591. Epub 2016 Nov 3.
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.
描述了一种在没有外部三氟甲基源的情况下将乙烯基三氟甲磺酸酯转化为α-三氟甲基化酮的新方法。该过程通过自由基过程实现三氟甲磺酸酯的三氟甲基基团在酮中的有效迁移到α-位。反应通过三氟甲基自由基加成到乙烯基三氟甲磺酸酯和随后的三氟甲烷磺酰基自由基的断裂进行。基于该反应,开发了酮的一锅两步三氟甲基化方法。本文所述的方法还允许从炔烃和全氟烷磺酸容易获得的乙烯基全氟烷磺酸盐中转移全氟烷基基团。