N-Aryl-N-phenylhydroxylamines were prepared from phenylmagnesium bromide and aryl nitro-compounds. The hydroxylamines were then reduced to secondary amines. The isolation of phenol as a by-product in the former reaction supports the suggested mechanism.
Y. Yost, H. R. Gutmann and C. C. Muscoplat, J. Chem. Soc. C, 1971, 2119 DOI: 10.1039/J39710002119
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