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Gem-dinitro compounds in organic synthesis. 4. Use of the condensation product of glyoxal and dinitromethane in the synthesis of nitro-1,2,3-triazoles
Authors:A. T. Baryshnikov  V. I. Erashko  N. I. Zubanova  B. I. Ugrak  S. A. Shevelev  A. A. Fainzilberg  V. V. Semenov
Abstract:
The condensation of dinitromethane with glyoxal has been investigated and it has been demonstrated that 1,1,4,4-tetranitro-2,3-butandiol, agr-hydroxy-beta,beta-dinitropropionic acid or their mixture may be formed. Interaction of 1,1,4,4-tetranitro-2,3-butandiol or 1,4-dibromo-1,1,4,4-tetranitro-2,3-butanediol diacetates with sodium azide leads to bis(5-nitro-1,2,3-triazol-4-yl) via intermediate 1,1,4,4-tetranitro-1,3-butadiene.For communication 3, see [1].N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 9, pp. 2123–2131, September, 1992.
Keywords:gem-dinitroethylenes  glyoxal  dinitromethane  dinitro compounds  nitro-1,2,3-triazoles  1,1,4,4-tetranitro-2,3-butandiol    /content/p0t67k13073214q3/xxlarge945.gif"   alt="  agr"   align="  BASELINE"   BORDER="  0"  >-hydroxy-  /content/p0t67k13073214q3/xxlarge946.gif"   alt="  beta"   align="  MIDDLE"   BORDER="  0"  >,  /content/p0t67k13073214q3/xxlarge946.gif"   alt="  beta"   align="  MIDDLE"   BORDER="  0"  >-dinitropropionic acid
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