AMINOBOROHYDRIDES .8. A FACILE REDUCTION OF ALIPHATIC AND BENZYLIC AZIDES TO THE CORRESPONDING AMINES IN HIGH-YIELD AND PURITY USING LITHIUM N,N-DIMETHYLAMINOBOROHYDRIDE
Sg. Alvarez et al., AMINOBOROHYDRIDES .8. A FACILE REDUCTION OF ALIPHATIC AND BENZYLIC AZIDES TO THE CORRESPONDING AMINES IN HIGH-YIELD AND PURITY USING LITHIUM N,N-DIMETHYLAMINOBOROHYDRIDE, Tetrahedron letters, 36(15), 1995, pp. 2567-2570
Lithium N,N-dimethylaminoborohydride (LiMe(2)NBH(3)) reduced both 3 al
pha-azidocholest-5-ene and 3 beta-azidocholest-5-ene in air to give th
e corresponding 3 alpha-aminocholest-5-ene and 3 beta-aminocholest-5-e
ne in 98% isolated yields. Aliphatic and benzylic azides were also red
uced with LiMe(2)NBH(3) to give the corresponding amines in isolated y
ields ranging from 85 to 98%. The reductions were complete in 1-3 hour
s and required only a simple acid-base extraction to isolate the desir
ed amines.