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Chemistry of Heterocyclic Compounds

, Volume 1, Issue 2, pp 173–176 | Cite as

Indole derivatives. XXIII. 3-Indolylethylene glycol

  • N. N. Suvorov
  • K. B. Kholodkovskaya
  • M. N. Preobrazhenskaya
Article
  • 59 Downloads

Abstract

Lithium aluminum hydride reduction at room temperature of 3-hydroxyacetylindole and 3-benzyloxyacetylindole in tetrahydrofuran gives, respectively, 3-indolyethyleneglycol and 3-indolylethylene glycol monobenzylate. Sodium borohydride reduction of 3-hydroxyacetylindole gives tryptophol, and the reduction of 3-benzyloxyacetylindole gives tryptophol benzylate. Aluminum amalgam converts 3-hydroxyacetylindole and 3-benzyloxyacetylindole to 3-acetylindole.

Keywords

Aluminum Lithium Glycol Hydride Indole 
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.

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Copyright information

© The Faraday Press, Inc. 1966

Authors and Affiliations

  • N. N. Suvorov
    • 1
  • K. B. Kholodkovskaya
    • 1
  • M. N. Preobrazhenskaya
    • 1
  1. 1.Ordzhonikidze All-Union Chemical-Pharmaceutical Scientific Research InstituteMoscow

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