Issue 86, 2014

A convenient method for producing mono- and dichlorohydrins from glycerol

Abstract

A new method for the transformation of glycerol into mono- and dichlorohydrins has been studied. With trimethylchlorosilane as chlorinating agent and acetic acid as catalyst, mono- and dichlorohydrins have been obtained in high yields and selectivity. In fact, under different reaction conditions, the synthesis of α-monochlorohydrin (3-chloropropan-1,2-diol) or α,γ-dichlorohydrin (1,3-dichloropropan-2-ol) as predominant product has been achieved. This process was also exploited for the valorisation of the crude mixture of glycerol and monochlorohydrin (glyceric mixture), a by-product from an earlier BioDiesel production. A reaction mechanism has been proposed based on investigations on the chlorination of different alcohols.

Graphical abstract: A convenient method for producing mono- and dichlorohydrins from glycerol

Article information

Article type
Paper
Submitted
06 Aug 2014
Accepted
05 Sep 2014
First published
08 Sep 2014

RSC Adv., 2014,4, 46319-46326

Author version available

A convenient method for producing mono- and dichlorohydrins from glycerol

D. Giomi, M. Malavolti, O. Piccolo, A. Salvini and A. Brandi, RSC Adv., 2014, 4, 46319 DOI: 10.1039/C4RA08240K

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