Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Letter
  • Published:

Acetylation of 4-Quinazolone

Abstract

THE sodium salt of 4-quinazolone1 is known to give 3-substituted derivatives on alkylation1. In the hope of preparing 3-acetyl-4-quinazolone, the sodium salt of 4-quinazolone was subjected to acetylation. When carefully dried sodium salt of 4-quinazolone was made to react with acetyl chloride in dry dioxane, a colourless crystalline compound C10H8O2N2, was isolated. The same derivative was obtained by refluxing 4-quinazolone with large excess of acetic anhydride. Extreme care was necessary in excluding water during the preparation and purification of this compound.

This is a preview of subscription content, access via your institution

Access options

Similar content being viewed by others

References

  1. Elderfield, R. C., “Heterocyclic Chemistry”, 6 (Wiley, 1958).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

MIRZA, R. Acetylation of 4-Quinazolone. Nature 186, 716–717 (1960). https://doi.org/10.1038/186716a0

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1038/186716a0

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing