Summary
-
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.
With the reaction with piperidine as example, it was shown to be possible to use 3,5-dialkyl-4-hydroxybenzyl bromides as alkylating agents.
Similar content being viewed by others
Literature cited
A. A. Volod'kin and V. V. Ershov, Izv. AN SSSR. Otd. khim. n. 1108 (1962).
C. Cook, N. Nash, and H. Flanagan, J. Amer. Chem. Soc.77. 1783 (1955).
O. Jacobsen, Liebigs Ann. Chem.195, 265 (1879).
K. Auwers and A. Schrenk, Liebigs Ann. Chem.344, 227 (1905).
V. V. Ershov and A. A. Volod'kin, Izv. AN SSSR. Otd. khim. n. 1290 (1962).
A. A. Volod'kin and V. V. Ershov, Izv. AN SSSR. Otd. khim. n. 342 (1962).
K. Fries and E. Brandes, Liebigs Ann. Chem.542, 48 (1939).
Author information
Authors and Affiliations
Additional information
The authors thank N. M. Émanuél' for constant interest in the work.
Rights and permissions
About this article
Cite this article
Volod'kin, A.A., Ershov, V.V. Sterically hindered phenols. Russ Chem Bull 11, 1213–1215 (1962). https://doi.org/10.1007/BF00908403
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00908403