Synthesis and certain conversions of 3-(3,3-dichloroallyl)-4-hydroxycoumarin

Authors

  • А. А. Аветисян Erevan State University, Erevan 375049
  • И. Л. Aлекcaнян Erevan State University, Erevan 375049
  • А. Г. Алвaнджян Erevan State University, Erevan 375049

Abstract

A method has been developed for the synthesis of 3-(3,3-dichloroallyl)-4-hydroxycoumarin and 2-thioxo-3-(3,3-dichloroallyl)-4-hydroxy-2H-chromene, and certain conversions of these compounds have been studied. They undergo acid hydrolysis readily, forming (respectively) 3-(4-hydroxy-3-coumarin)- and 3-(2-thioxo-4-hydroxy-2H-chromene-3)propionic acids; these compounds are converted to the corresponding lactones by the action of acetic anhydride.

How to Cite
Avetisyan, A. A.; Aleksanyan, I. L.; Alvandzhyan, A. G. Chem. Heterocycl. Compd. 1997, 33, 39. [Khim. Geterotsikl. Soedin. 1997, 48.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02290744

Published

1997-01-25

Issue

Section

Original Papers