Difluoromethyl 2-pyridyl sulfone (
1), which is composed of pyridyl and difluoromethylsulfonyl groups, performs as a difluoromethylating reagent when used with metal catalysts. For example, Hu
et al. have reported that
1 reacts with aryl zinc reagents(
2) in the presence of
tris(2,4-pentanedionato)iron(III) and
tetramethylenediamine(TMEDA) giving the corresponding difluoromethylated aryl products in good yields. This reaction can be applied to various aryl group substituted zinc compounds such as a phenyl group and others like methoxy-, trifluoromethyl-, or heteroaryl-substituted aryl groups. In this way,
1 is expected to be used directly as a difluoromethylating reagent introducing a difluoromethyl group into aryl groups.