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


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.


Hydrogenation Organic Chemistry Furan Propyl Furfural 
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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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