Chemistry of Heterocyclic Compounds

, Volume 10, Issue 9, pp 1042–1044 | Cite as

Kinetics of the alkaline hydrolysis of 3-sulfolanol phenyl ethers

  • T. É. Bezmenova
  • A. F. Rekasheva
  • T. S. Lutskii
  • R. A. Dorofeeva


A scheme for the elimination of aryloxy groups via an ElcB mechanism is proposed on the basis of data on the kinetics of the alkaline hydrolysis of 3-sulfolanol phenyl ethers in H2O and D2O.


Ether Hydrolysis Organic Chemistry Phenyl Alkaline Hydrolysis 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.


Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature cited

  1. 1.
    T. É. Bezmenova, R. A. Dorofeeva, and A. Ya. Bezmenov, Zh. Organ. Khim., 3, 778 (1967).Google Scholar
  2. 2.
    T. É. Bezmenova, Yu. N. Usenko, A. F. Rekasheva, I. S. Lushnik, and A. V. Misyura, Khim. Geterotsikl. Soedin., 767 (1972).Google Scholar
  3. 3.
    G. Crosby and C. J. Stirling, J. Chem. Soc., B, 679 (1970).Google Scholar
  4. 4.
    Z. Rappoport, J. Chem. Soc., B, 171 (1971).Google Scholar
  5. 5.
    W. Pritzkow, Wiss. Zeit., 12, 213 (1970).Google Scholar
  6. 6.
    C. D. Ritchie and W. F. Sager, Progr. Phys. Org. Chem., 3, 323 (1965).Google Scholar
  7. 7.
    L. R. Fedor, J. Amer. Chem. Soc., 91, 908 (1969).Google Scholar
  8. 8.
    L. Fedor and W. R. Clave, J. Amer. Chem. Soc., 93, 985 (1971).Google Scholar
  9. 9.
    A. J. Evans and S. D. Hamann, Trans. Faraday Soc., 47, 34 (1952).Google Scholar

Copyright information

© Plenum Publishing Corporation 1976

Authors and Affiliations

  • T. É. Bezmenova
    • 1
  • A. F. Rekasheva
    • 1
  • T. S. Lutskii
    • 1
  • R. A. Dorofeeva
    • 1
  1. 1.Institute of the Chemistry of High-Molecular-Weight CompoundsAcademy of Sciences of the Ukrainian SSRKiev

Personalised recommendations