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Synthesis of Ethophenprox

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Abstract

An ethophenprox synthesis from easily available p-nitroneophyl chloride was developed. The reduction of the latter to aniline derivative followed by Sandmayer's and Claisen's reactions furnished p-ethoxyneophyl chloride that by condensation with 3-phenoxybenzyl alcohol in the presence KOH in DMSO yielded ethophenprox.

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Authors and Affiliations

  1. Institute of Organic Chemistry, Ufa Scientifc Center, Russian Academy of Sciences, Ufa, 450054, Russia

    R. G. Rakhimov, F. Z. Galin & Yu. V. Tomilov

  2. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, 197034, Russia

    V. T. Le

Authors
  1. R. G. Rakhimov
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  2. F. Z. Galin
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  3. Yu. V. Tomilov
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  4. V. T. Le
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Rakhimov, R.G., Galin, F.Z., Tomilov, Y.V. et al. Synthesis of Ethophenprox. Russian Journal of Organic Chemistry 38, 1629–1634 (2002). https://doi.org/10.1023/A:1022562101602

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