ABSTRACT
Ortho-, meta- and para-isomers of (3,3,3-trifluoropropyl)aniline have been prepared in 60–70 g amount from the corresponding nitrobenzaldehydes in three steps.
from The key synthesis step was a transformation of thecarboxylicgroupof
3-(nitrophenyl)propanoicacidsintothetrifluoromethylgroupbySF