Abstract

Abstract The reaction of phenylcarbamoyl cyanide with LiAlH4 or NaBH4 gave glycine anilide, N-phenylethylenediamine, and N-methylaniline. With the latter hydride, 4-amino-1,3-diphenyl-2-imidazolidinone was also formed. The reduction of diphenylcarbamoyl cyanide with LiAlH4 gave N-methyldiphenylamine as the only reduction product.

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