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Mendeleev Communications, 1998, Volume 8, Issue 2, Pages 69–70
DOI: https://doi.org/10.1070/MC1998v008n02ABEH000896
(Mi mendc4659)
 

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).
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Document Type: Article
Language: English


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
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  • This publication is cited in the following 18 articles:
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