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Chemistry of Heterocyclic Compounds

, Volume 28, Issue 3, pp 297–298 | Cite as

Catalytic method of synthesis of 2,4-diphenylfuran and 2-phenylindole

  • B. N. Anisimov
  • A. A. Obynochnyi
  • N. S. Prostakov
Article
  • 46 Downloads

Abstract

2,4-Diphenylfuran has been obtained from acetophenone and its mixture with aniline, over K-16 catalyst. It has been established that the reaction proceeds through a stage of dypnone formation. When the aniline-acetophenone mixture is used as the starting material, small amounts of 2-phenylindole are formed.

Keywords

Organic Chemistry Aniline Acetophenone Catalytic Method Dypnone 
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.

Literature cited

  1. 1.
    N. S. Prostakov and A. V. Varlamov, Khim. Geterotsikl. Soedin., No. 11, 1011 (1988).Google Scholar
  2. 2.
    Beilstein Handbuch, Vol. 7, Berlin (1925), p. 465.Google Scholar
  3. 3.
    K. Weygand and H. Hilgetage, Methods of Experiment in Organic Chemistry [Russian translation], Khimiya, Moscow (1968), p. 886.Google Scholar

Copyright information

© Plenum Publishing Corporation 1992

Authors and Affiliations

  • B. N. Anisimov
    • 1
  • A. A. Obynochnyi
    • 1
  • N. S. Prostakov
    • 1
  1. 1.P. Lumumba University of People's FriendshipUSSR

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