A NOVEL TRANSFORMATION OF ESTERS TO ALKYNES WITH 1-SUBSTITUTED BENZOTRIAZOLES

Reactions of lithio benzotriazol-1-yl derivatives 2, 11, and 25 with a romatic and aliphatic esters 3, 12, and 26 gave alpha-(benzotriazol-1- yl) ketones 4, 13, and 27, respectively, in high yields. Alternatively , alpha-(benzotriazol-1-yl) ketones 22 can be accessed by the reaction of alpha-(benzotriazol-1-yl) esters 20 with Grignard reagents. Conden sation of 4, 13, 22, and 27 with (p-toluenesulfonyl)hydrazine provided p-tosylhydrazones 5, 14, 21, and 28. Treatment of hydrazones 5, 21, a nd 28 with n-butyllithium in diethyl ether resulted in the elimination of the tosyl group, dinitrogen, and benzotriazolyl group to afford th e corresponding acetylenes 9, 23, and 29 in good yields. When alpha-(b enzotriazol-1-yl) 1-alpha-phenoxy hydrazones 14 were treated with meth yllithium, n-butyllithium, or phenyllithium, alkynes 18 were obtained, in which phenoxy groups were replaced by the lithium reagents.