Issue 2, 1998

Reaction of glycidol with dichloroethers: cyclic and acyclic ortho ester formation

Abstract

The interaction of stoichiometric quantities of glycidol with alkyl dichloromethyl ethers in the presence of 2 equiv. of NEt3 in diethyl ether leads to formation of diglycidyloxy alkoxy methanes whereas the same reaction involving equimolar quantities of the reagents in benzene in the presence of 1 equiv. of NEt3 leads to formation of 4-chloromethyl-2-alkoxy-1,3-dioxolanes.

Article information

Article type
Paper

Mendeleev Commun., 1998,8, 81-82

Reaction of glycidol with dichloroethers: cyclic and acyclic ortho ester formation

A. A. Bredikhin and S. N. Lazarev, Mendeleev Commun., 1998, 8, 81 DOI: 10.1070/MC1998v008n02ABEH000919

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