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Chemistry of Heterocyclic Compounds

, Volume 4, Issue 4, pp 442–443 | Cite as

Furan compounds

XXXIV. Reductive amination of furan aldehydes with monoethanolamine
  • A. A. Ponomarev
  • E. A. Zadumina
  • I. A. Markushina
  • I. M. Skvortsov
Article
  • 57 Downloads

Abstract

By reductive amination, starting from furfural, 5-methylfurfural, β-(2-furyl)acrolein, and monoethanolamine, we have obtained N-furfurylaminoethanol, N-(5-methyl-2-furfuryl)aminoethanol, and N-[1-(α-furyl)-3-propyl]aminoethanol. By reductive amination combined with the subsequent hydrogenation of the furan ring we have obtained N-tetrahydrofurfurylaminoethanol and N-(5-methyltetrahydro-2-furfuryl)aminoethanol.

Keywords

Hydrogenation Organic Chemistry Furan Propyl Furfural 
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

© Consultants Bureau 1971

Authors and Affiliations

  • A. A. Ponomarev
    • 1
  • E. A. Zadumina
    • 1
  • I. A. Markushina
    • 1
  • I. M. Skvortsov
    • 1
  1. 1.Chernyshevskii Saratov State UniversityUSSR

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