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Reactivity of allyl aryl ethers in diene condensation with hexachlorocyclopentadiene

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Abstract

The reactivity of allyl aryl ethers in the diene condensation with hexachlorocyclopentadiene was studied. The reactivity of aryl allyl ethers and product yield in this reaction significantly decreases when electron-withdrawing groups are introduced into the benzene ring. The reactivity is also influenced by the temperature, reaction time, and the molar ratio of the diene and dienophile.

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Authors and Affiliations

  1. Kuliev Institute of Chemistry of Additives of National Academy of Sciences of Azerbaijan, Beyukshorskoye sh. 2062, Baku, AZ-1029, Azerbaijan

    B. I. Musaeva, N. N. Novotorzhina, G. A. Gakhramanova & I. P. Ismailov

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  1. B. I. Musaeva
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  2. N. N. Novotorzhina
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  3. G. A. Gakhramanova
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  4. I. P. Ismailov
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Correspondence to B. I. Musaeva.

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Original Russian Text © B.I. Musaeva, N.N. Novotorzhina, G.A. Gakhramanova, I.P. Ismailov, 2012, published in Zhurnal Obshchei Khimii, 2012, Vol. 82, No. 12, pp. 2024–2027.

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Musaeva, B.I., Novotorzhina, N.N., Gakhramanova, G.A. et al. Reactivity of allyl aryl ethers in diene condensation with hexachlorocyclopentadiene. Russ J Gen Chem 82, 1978–1981 (2012). https://doi.org/10.1134/S1070363212120122

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  • DOI: https://doi.org/10.1134/S1070363212120122

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