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Sterically hindered phenols

Communication 5. Quinobenzyl rearrangement of quinobromides

  • Organic and Biological Chemistry
  • Published:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    The rearrangements of quinobromides prepared from 2,4,6-trialkylphenols (2,4,6-trialkyl-4-bromo-2,5cyclohexadien-1-ones) into 3,5-dialkyl-4-hydroxybenzyl bromides were carried out.

  2. 2.

    With the reaction with piperidine as example, it was shown to be possible to use 3,5-dialkyl-4-hydroxybenzyl bromides as alkylating agents.

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Literature cited

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The authors thank N. M. Émanuél' for constant interest in the work.

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Volod'kin, A.A., Ershov, V.V. Sterically hindered phenols. Russ Chem Bull 11, 1213–1215 (1962). https://doi.org/10.1007/BF00908403

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  • DOI: https://doi.org/10.1007/BF00908403

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