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N-(alkoxycarbonylmethyl)diazene-N-oxides and some of their conversions

  • Organic Chemistry
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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Abstract

Upon reaction of aliphatic and aromatic nitroso compounds with esters of N,N-dibromoglycine N-substituted N-(alkoxycarbonylmethyl)diazene-N-oxides are formed. The ethyl ester of (2-phenyldiazene-2-oxido)acetic acid in concentrated H2SO4 is transformed into a mixture of the monophenylhydrazide and monophenylhydrazone of monoethyl oxalate and in a solution of gaseous HCl in acetic acid into the phenylhydrazone of the acyl chloride of monoethyl oxalate.

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 2, pp. 352–356, February, 1990.

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Luk'yanov, O.A., Salamonov, Y.B., Bass, A.G. et al. N-(alkoxycarbonylmethyl)diazene-N-oxides and some of their conversions. Russ Chem Bull 39, 294–297 (1990). https://doi.org/10.1007/BF00960656

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  • DOI: https://doi.org/10.1007/BF00960656

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