Advertisement

Heterocyclic compounds

Part XII. Chromones from resacyl and gallacylphenones containing long-chain acylgroups, and some chemical properties of these hydroxy-ketones
  • R. D. Desai
  • W. S. Waravdekar
Article
  • 11 Downloads

Summary

Resorcinol and pyrogallol have been condensed with stearic, palmitic and lauric acids to obtain the dihydroxy and trihydroxy ketones. Chromones have been prepared from them, and it is observed that the resulting γ-pyrones gave only the orignial ketones on alkaline hydrolysis, and not a trace of theo-hydroxy-carboxylic acids. As most of these ketones were prepared for the first time, their bromination, nitration and reduction were studied. The last reaction gave resorcinols and pyrogallols containing octadecyl, hexadecyl and dodecyl-groups in the 4-position.

Keywords

Ferric Chloride Resorcinol Lauric Acid Alkaline Hydrolysis Pyrogallol 
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.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. 1.
    Desai and Waravdekar,Proc. Ind. Acad. Sci. (A), 1940,12, 507.Google Scholar
  2. 2.
    Heilbron and co-workers,J., 1933, 1263; 1934, 1311, 1581; 1936, 295.Google Scholar
  3. 3.
    Klarmann,Jour. Amer. Chem. Soc., 1926,48, 2358.CrossRefGoogle Scholar

Copyright information

© Indian Academy of Sciences 1941

Authors and Affiliations

  • R. D. Desai
    • 1
  • W. S. Waravdekar
    • 1
  1. 1.Chemistry DepartmentSt. Xavier’s CollegeBombay

Personalised recommendations