Issue 13, 1984

An unexpected outcome of a general thiazole synthesis

Abstract

The reaction between N-benzoyl-N′-methyl-N′-phenylthiourea and chloroacetone gives 5-benzoyl-4-methyl-2-(N-methyl-N-phenylamino)thiazole rather than the 5-acetyl-4-phenylisomer which would be predicted from previous work on this route to thiazoles.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 837-838

An unexpected outcome of a general thiazole synthesis

G. D. Meakins, M. D. J. Padgham, N. Patel and J. M. Peach, J. Chem. Soc., Chem. Commun., 1984, 837 DOI: 10.1039/C39840000837

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements