Reactions of N-hydroxy-amines with sulphuryl chloride in ether gave N-chloro-N-hydroxyammonium salts. Work-up of these salts with aqueous potassium hydroxide afforded nitrones or nitrosobenzenes, depending on the starting materials. Reactions in acetonitrile, in which the intermediate salts are soluble, yielded products of further reaction of the nitrones.
M. Nojima, K. Takeuchi, E. Fukui and N. Tokura, J. Chem. Soc., Perkin Trans. 1, 1976, 2202 DOI: 10.1039/P19760002202
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...