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Regioselective alkylation of isopropylidene- and cyclohexylidenepropanedinitrile with phenacyl bromides

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Abstract

Alkylation of isopropylidene- and cyclohexylidenepropanedinitrile with phenacyl bromides gave 2,2-bis(2-aryl-2-oxoethyl)propanedinitriles. Direct alkylation of propanedinitrile with phenacyl bromides afforded only 2-(2-aryl-2-oxoethyl)propanedinitriles.

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Authors and Affiliations

  1. Taras Shevchenko Lugansk University, ul.Oboronnaya 2, Lugansk, 91011, Ukraine

    V. D. Dyachenko & A. N. Pavlova

Authors
  1. V. D. Dyachenko
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  2. A. N. Pavlova
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Correspondence to V. D. Dyachenko.

Additional information

Original Russian Text © V.D. Dyachenko, A.N. Pavlova, 2015, published in Zhurnal Organicheskoi Khimii, 2015, Vol. 51, No. 12, pp. 1728–1731.

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Dyachenko, V.D., Pavlova, A.N. Regioselective alkylation of isopropylidene- and cyclohexylidenepropanedinitrile with phenacyl bromides. Russ J Org Chem 51, 1693–1696 (2015). https://doi.org/10.1134/S1070428015120040

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  • DOI: https://doi.org/10.1134/S1070428015120040

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