Issue 0, 1972

Synthesis of ethyl 3-oxopyrazolidine-4-carboxylates

Abstract

Ethyl 3-oxopyrazolidine-4-carboxylates are formed in reactions of hydrazine hydrate with αβ-unsaturated diesters or with β-anilino-diesters. The usefulness of the method is limited by the occurrence of other reactions, notably cleavage of the diesters (to malonohydrazide and the appropriate aldehyde azine); ethyl 3-hydroxypyrazole-4-carboxylate derivatives are also produced, subsequent to formation of the oxopyrazolidines.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 1416-1419

Synthesis of ethyl 3-oxopyrazolidine-4-carboxylates

C. N. O'Callaghan, J. Chem. Soc., Perkin Trans. 1, 1972, 1416 DOI: 10.1039/P19720001416

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