Copper-catalyzed trifluoromethylation of internal olefinic C-H bonds: efficient routes to trifluoromethylated tetrasubstituted olefins and N-heterocycles.

The functionalization of internal olefins has been a challenging task in organic synthesis. Efficient Cu-II-catalyzed trifluoromethylation of internal olefins, that is, -oxoketene dithioacetals, has been achieved by using Cu(OH)(2) as a catalyst and TMSCF3 as a trifluoromethylating reagent. The push-pull effect from the polarized olefin substrates facilitates the internal olefinic CH trifluoromethylation. Cyclic and acyclic dithioalkyl -oxoketene acetals were used as the substrates and various substituents were tolerated. The internal olefinic CH bond cleavage was not involved in the rate-determining step, and a mechanism that involves radicals is proposed based on a TEMPO-quenching experiment of the trifluoromethylation reaction. Further derivatization of the resultant CF3 olefins led to multifunctionalized tetrasubstituted CF3 olefins and trifluoromethylated N-heterocycles.