C. M. Darling, C. P. Chen
Jun 1, 1978
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0
Influential Citations
1
Citations
Journal
Journal of pharmaceutical sciences
Abstract
The reduction of N-benzyl-2-cyano-2-(hydroxyimino)acetamide resulted in the formation of N-benzyl-1,2-ethanediamine and N-benzyl-N'-methyl-1,2-ethanediamine in approximately an equimolar ratio. The formation of the two unexpected products is explained by the migration of a cyano group in a Beckmann-type rearrangement.