Issue 8, 1970

Reaction of t-butylamine with cyclohexane-1,3-dione

Abstract

When t-butylamine reacts with cyclohexane-1,3-dione in refluxing xylene the first product is a dehydrated dimer of the diketone which then reacts with the base. The nature of the yellow final product is discussed on the basis of u.v., pKa and n.m.r. data.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 1002-1004

Reaction of t-butylamine with cyclohexane-1,3-dione

J. V. Greenhill, J. Chem. Soc. C, 1970, 1002 DOI: 10.1039/J39700001002

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