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Chemistry of Heterocyclic Compounds

, Volume 9, Issue 7, pp 802–804 | Cite as

Mono- and dihalogenofurfurals in the wittig reaction

  • Z. N. Nazarova
  • I. I. Popov
  • A. M. Simonov
  • A. P. Kravtsova
  • S. S. Goryaev
Article

Abstract

The reaction of 3(5)-monohalogeno- and 4,5-dihalogenofurfurals with alkoxycarbonylmethyl-enetriphenylphosphoranes has given esters of β- [3(5)-mono- and -4,5-dihalogeno-2-furyl]-acrylic acids, which are converted by alkaline hydrolysis into the corresponding halogen-substituted furylacrylic acids.

Keywords

Ester Hydrolysis Organic Chemistry Acrylic Acid 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.

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Copyright information

© Plenum Publishing Corporation 1975

Authors and Affiliations

  • Z. N. Nazarova
    • 1
  • I. I. Popov
    • 1
  • A. M. Simonov
    • 1
  • A. P. Kravtsova
    • 1
  • S. S. Goryaev
    • 1
  1. 1.Rostov State UniversityRostov-on-Don

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