Issue 31, 2008

From 1,2-dialkoxyalkanes to 1,4-dioxanes. A transformation mediated by NbCl5via multiple C–O bond cleavage at room temperature

Abstract

The formation of 1,4-dioxanes and alkyl chlorides from the reactions of polyethers (dme, diglyme, 1,2-diethoxyethane, 1,2-dimethoxypropane) with NbCl5 at room temperature is described; as far as dme is concerned, the reaction mainly occurs in two steps, consisting of (i) cleavage of one O–CH3 bond, followed by (ii) cleavage of the second O–CH3 bond and one of the two O–CH2 linkages. The characterization of intermediate complexes and the isolation of NbOCl3(dme) are reported.

Graphical abstract: From 1,2-dialkoxyalkanes to 1,4-dioxanes. A transformation mediated by NbCl5via multiple C–O bond cleavage at room temperature

Supplementary files

Article information

Article type
Communication
Submitted
14 Mar 2008
Accepted
28 Apr 2008
First published
09 Jun 2008

Chem. Commun., 2008, 3651-3653

From 1,2-dialkoxyalkanes to 1,4-dioxanes. A transformation mediated by NbCl5via multiple C–O bond cleavage at room temperature

F. Marchetti, G. Pampaloni and S. Zacchini, Chem. Commun., 2008, 3651 DOI: 10.1039/B804432E

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.

Social activity

Spotlight

Advertisements