The azidonitration of tri-O-acetyl-D-galactal

Reaction of 3,4,6-tri-O-acetyl- D -galactal with excess ceric ammonium nitrate and sodium azide in acetonitrile produced 2-azido-1-nitrate addition products (53% β-galacto, 22% α-galacto, and 8% α-talo) and N-acetyl-3,4,6-tri-O-acetyl-2-azido-2-deoxy-α- D -galactopyranosylamine was formed, on hydrolysis, in 10% yield. The reaction product provides a convenient source of D -galactosamine and 3,4,6-tri-O-acetyl-2-azido-2-deoxy-α- D -galactopyranosylhalides. The crystalline β-chloride is also reported. The use of these glycosyl halides as reactants for the preparation of 2-azido-2-deoxy-α- and -β- D -galactopyranosides under conditions promoted by both mercuric cyanide and silver salts are reported.