Abstract
The reductive coupling of 4-bromo-3,3,4,4-tetrafluorobut-1-ene
with 2.4 equivalents of various carbonyl compounds proceeded very
smoothly in the presence of 2.4 equivalents of MeLi/LiBr-free
at -78 ˚C for two hours, giving the corresponding adducts
in high to excellent yields. On the other hand, triethyl(1,1,2,2-tetrafluorobut-3-enyl)silane,
which could be prepared by treatment of 4-bromo-3,3,4,4-tetrafluorobut-1-ene
and chlorotriethylsilane with magnesium at 0 ˚C for three
hours, reacted with some aldehydes in the presence of 1 mol% of
tetrabutylammonium fluoride, the desired adducts being obtained
in good to high yields.
Key words
tetrafluoroethylene - MeLi/LiBr-free - triethyl(1,1,2,2-tetrafluorobut-3-enyl)silane - reductive coupling