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Synthesis of 2,3-Diphenylacrolein Acetals

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Abstract

Linear acetals have been synthesized by decomposition trans- and cis-1,1-dichloro-2,3-diphenylcyclopropanes in the presence of aliphatic alcohols (ethanol and butan-1-ol). The reactivities of pure trans- and cis-stilbenes and styrene toward dichlorocarbene have been compared. The structure of the isolated compounds was determined by NMR and GC/MS.

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Funding

This study was performed under financial support by the President of the Russian Federation (program for state support of young Russian candidates and doctors of science, project no. MK-1689.2020.3).

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Authors and Affiliations

  1. Ufa State Petroleum Technological University, 450062, Ufa, Russia

    G. N. Sakhabutdinova, G. Z. Raskilʼdina & S. S. Zlotskii

Authors
  1. G. N. Sakhabutdinova
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  2. G. Z. Raskilʼdina
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  3. S. S. Zlotskii
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Corresponding author

Correspondence to G. Z. Raskilʼdina.

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Sakhabutdinova, G.N., Raskilʼdina, G.Z. & Zlotskii, S.S. Synthesis of 2,3-Diphenylacrolein Acetals. Russ J Gen Chem 90, 1750–1752 (2020). https://doi.org/10.1134/S1070363220090248

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  • DOI: https://doi.org/10.1134/S1070363220090248

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