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Alkoxyhalogenation of Dichlorostyrenes in Unsaturated C3-Alcohols

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Abstract

Alkoxyhalogenation of dihalostyrenes with allyl or propargyl alcohol and N-bromosuccinimide or crystalline iodine in the presence of clinoptilolite [(NaK)4CaAl6Ci30O72] afforded the corresponding unsaturated β-halo ethers with high yields.

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Authors and Affiliations

  1. Mamedaliyev Institute of Petrochemical Processes, National Academy of Sciences of Azerbaijan, Baku, 1025, Azerbaijan

    G. M. Talybov, A. R. Ezizbeyli & E. Q. Mammadbayli

  2. Azerbaijan State Oil and Industrial University, Baku, 1010, Azerbaijan

    G. R. Gurbanov

Authors
  1. G. M. Talybov
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  2. A. R. Ezizbeyli
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  3. E. Q. Mammadbayli
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  4. G. R. Gurbanov
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Corresponding authors

Correspondence to G. M. Talybov or G. R. Gurbanov.

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The authors declare the absence of conflict of interest.

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Russian Text © The Author(s), 2020, published in Zhurnal Organicheskoi Khimii, 2020, Vol. 56, No. 1, pp. 47–51.

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Talybov, G.M., Ezizbeyli, A.R., Mammadbayli, E.Q. et al. Alkoxyhalogenation of Dichlorostyrenes in Unsaturated C3-Alcohols. Russ J Org Chem 56, 34–37 (2020). https://doi.org/10.1134/S1070428020010066

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  • DOI: https://doi.org/10.1134/S1070428020010066

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