Issue 21, 2020

Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides

Abstract

A series of bifunctional phase-transfer catalysts (PTCs) were synthesized to catalyze the [3 + 2] coupling reaction of isocyanates and epoxides to afford 2-oxazolidinones in good to high yields (up to 92% yield) using PhCl as a solvent at 100 °C within 12 h. These bifunctional PTCs were easily prepared from commercially available tertiary-primary diamines and isocyanates (or isothiocyanates, mono-squaramides, respectively) in two simple steps with good modularity and demonstrated high efficiency (2.5 mol% catalyst-loading). The synergistic interaction of the quaternary ammonium salt center and hydrogen-bond donor group in the catalyst with the substrate is crucial to this atom-economic reaction.

Graphical abstract: Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides

Supplementary files

Article information

Article type
Paper
Submitted
22 Jan 2020
Accepted
19 Mar 2020
First published
26 Mar 2020
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2020,10, 12360-12364

Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides

D. Cui, Y. Li, P. Huang, Z. Tian, Y. Jia and P. Wang, RSC Adv., 2020, 10, 12360 DOI: 10.1039/D0RA00693A

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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