A single-stage synthesis of methyl and ethyl N-benzoyl-4-piperidone-3-carboxylates from benzamide and the appropriate alkyl acrylate is reported. The esters have been directly converted into N-benzoyl-4-piperidone. The use of t-butyl esters in the Dieckmann synthesis of N-phenyl-4-piperidone-3-carboxylates leads to an increased yield of N-phenyl-4-piperidone.
J. D. Baty, G. Jones and C. Moore, J. Chem. Soc. C, 1967, 2645 DOI: 10.1039/J39670002645
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.
Please wait while we load your content...