Herein, inorganic base K3PO4 promoted
divergent
synthesis of CF3-substituted allenes, cyclopentenes, alkynes,
and fluorinated enynes via regioselective nucleophilic addition of
carbon nucleophiles to 2-trifluoromethyl-1,3-enynes was developed.
With the choice of different carbon nucleophiles, various fluorinated
compounds could be obtained under K3PO4/DMF
reaction system. When malononitriles were used as nucleophiles, CF3-substituted allenes, cyclopentenes, and alkynes could be
obtained, respectively. By using 1,3-dicarbonyl compounds as nucleophiles,
ring-monofluorinated 4H-pyrans could be prepared,
and 1,1-difluoro-1,3-enynes could be furnished with the participation
of diethyl malonate. Moreover, these five kinds of fluorinated allenes,
alkenes, and enynes are valuable building blocks.