The key intermediate to 3,3-difluoroalanine, 2,2-difluoro-1-ethyl-thio
ethylamine hydrobromide (2), was prepared by the Steglich and Weygand
procedure. Its conversion to benzyloxycarbonyl-2,2-difluoro-1-ethenyle
thylamine (5) followed by oxidation and subsequent deprotection of the
amine afforded the 3,3-difluoroalanine.