The reactions of hexafluoropropylene, its dimers and trimers, and perf
luoro-1-ethylcyclo-hex-1-ene with secondary amines (dipropylamine, dib
utylamine and diallylamine) have been shown to form enamines. The enam
ines were electrochemically fluorinated in anhydrous hydrogen fluoride
. This paper reports the electrochemical fluorination data for the flu
orination of tripropylamine, tributylamine, triamylamine and the parti
ally fluorinated enamines. The structures of the products have been co
nfirmed by F-19 NMR and GC-MS methods.