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Synthesis of hexachlorobicyclo[2.2.1]hept-5-enylmethyl haloacetates

  • Organic Synthesis and Industrial Organic Chemistry
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Abstract

The possibility of preparing hexachlorobicyclo[2.2.1]hept-5-enylmethyl haloacetates by reactions of hexachlorocyclopentadiene with allyl haloacetates was examined. The optimal conditions for preparing the esters were found. The structures of the compounds prepared were proved by IR and 1H NMR spectroscopy.

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Authors and Affiliations

  1. Institute of Chemical Problems, National Academy of Sciences of Azerbaijan, Baku, Azerbaijan

    E. G. Mamedbeili (Mamedov), T. G. Kyazimova, Kh. I. Gasanov, O. B. Abdiev & I. M. Mamedova

  2. Institute of Petrochemical Processes, National Academy of Sciences of Azerbaijan, Baku, Azerbaijan

    E. G. Mamedbeili (Mamedov), T. G. Kyazimova, Kh. I. Gasanov, O. B. Abdiev & I. M. Mamedova

Authors
  1. E. G. Mamedbeili (Mamedov)
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  2. T. G. Kyazimova
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  3. Kh. I. Gasanov
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  4. O. B. Abdiev
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  5. I. M. Mamedova
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Additional information

Original Russian Text © E.G. Mamedbeili (Mamedov), T.G. Kyazimova, Kh.I. Gasanov, O.B. Abdiev, I.M. Mamedova, 2009, published in Zhurnal Prikladnoi Khimii, 2009, Vol. 82, No. 2, pp. 288–292.

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Mamedbeili (Mamedov), E.G., Kyazimova, T.G., Gasanov, K.I. et al. Synthesis of hexachlorobicyclo[2.2.1]hept-5-enylmethyl haloacetates. Russ J Appl Chem 82, 282–286 (2009). https://doi.org/10.1134/S1070427209020220

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  • DOI: https://doi.org/10.1134/S1070427209020220

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