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Reactions of 1-bromo-1-nitro-3,3,3-trichloropropene with acetylacetone and cyclohexane-1,3-dione

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Abstract

Reactions of 1-bromo-1-nitro-3,3,3-trichloropropene with acetylacetone, dihydroresorcinol, and dimedone afforded substituted dihydrofuran and hexahydrobenzofurans containing nitro and trichloromethyl functionalities. Their structure was established by spectroscopic (IR, UV, 1H, 13C–{1H} NMR) methods and X-ray diffraction analysis.

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Authors and Affiliations

  1. Herzen State Pedagogical University of Russia, nab. reki Moiki 48, St. Petersburg, 191186, Russia

    S. V. Makarenko, E. V. Trukhin & V. M. Berestovitskaya

  2. Elastokam, St. Petersburg, Russia

    E. V. Stukan’

Authors
  1. S. V. Makarenko
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  2. E. V. Stukan’
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  3. E. V. Trukhin
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  4. V. M. Berestovitskaya
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Corresponding author

Correspondence to S. V. Makarenko.

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Original Russian Text © S.V. Makarenko, E.V. Stukan’, E.V. Trukhin, V.M. Berestovitskaya, 2015, published in Zhurnal Obshchei Khimii, 2015, Vol. 85, No. 10, pp. 1659–1662.

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Makarenko, S.V., Stukan’, E.V., Trukhin, E.V. et al. Reactions of 1-bromo-1-nitro-3,3,3-trichloropropene with acetylacetone and cyclohexane-1,3-dione. Russ J Gen Chem 85, 2291–2294 (2015). https://doi.org/10.1134/S1070363215100126

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  • DOI: https://doi.org/10.1134/S1070363215100126

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