Unlike its hydrocarbon counterpart, perfluoro-2-(trifluoromethyl)prope
ne is a highly reactive compound. It participates in both heterolytic
and homolytic reactions. It readily reacts with nucleophiles and slugg
ishly with electrophiles. It reacts as well with common organic solven
ts, such as dimethylformamide, ethanol and others. In this communicati
on, we describe its reactions with trifluoromethylthiocopper, sulfur t
rioxide and tributyltin cyanide, the mechanism of formation of the var
ious products and their mass spectral data.