Abstract
Reaction of 1-methyl-3,5-dinitro-1,2,4-triazole with alcohols or phenols in the presence of bases (tertiary amines) leads to replacement of the nitro group in the 5-position by an alkoxy or phenoxy group.
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L. I. Bagal and M. S. Pevzner, KhGS [Chemistry of Heterocyclic Compounds], 558, 1970.
K. Gastaldi, Gazz. chim. ital., 53, 629, 1923.
E. Hoggarth, J. Chem. Soc., 1918,1949.
L. I. Bagal, M. S. Pevzner, and V. Ya. Samarenko, KhGS [Chemistry of Heterocyclic Compounds], 269, 1970.
L. I. Bagal, M. S. Pevzner, N. I. Sheludyakova, and V. M. Kerusov, KhGS [Chemistry of Heterocyclic Compounds], 265, 1970.
A. Cross, Introduction to Practical Infrared Spectroscopy [Russian translation], IL, Moscow, 1964, p. 102.
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For part IV, see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, Vol. 6, No. 5, pp. 702–704, May, 1970.
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Bagal, L.I., Pevzner, M.S., Samarenko, V.Y. et al. Heterocyclic nitro compounds. Chem Heterocycl Compd 6, 650–652 (1970). https://doi.org/10.1007/BF00500695
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DOI: https://doi.org/10.1007/BF00500695