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This article is cited in 18 scientific papers (total in 18 papers)
Replacement of the nitro groups in 1,3,5-trinitrobenzene on treatment with polyfluorinated alcohols
S. A. Sheveleva, M. D. Dutova, M. A. Koroleva, O. Yu. Sapozhnikova, A. L. Rusanovb a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Abstract:
Depending on the conditions, polyfluorinated alcohols RfCH2OH [Rf = CF3, H(CF2)n; n = 2, 4, 6, 8] replace one or two nitro groups in 1,3,5-trinitrobenzene in the presence of K2CO3 in N-methylpyrrolidone to give the previously unknown 1-polyfluoroalkoxy-3,5-dinitrobenzenes or 1,3-di(polyfluoroalkoxy)-5-nitrobenzenes; the reaction is successful due to the high acidity of RfCH2OH (pKa ≈ 12).
Citation:
S. A. Shevelev, M. D. Dutov, M. A. Korolev, O. Yu. Sapozhnikov, A. L. Rusanov, “Replacement of the nitro groups in 1,3,5-trinitrobenzene on treatment with polyfluorinated alcohols”, Mendeleev Commun., 8:2 (1998), 69–70
Linking options:
https://www.mathnet.ru/eng/mendc4659 https://www.mathnet.ru/eng/mendc/v8/i2/p69
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