Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
170631 | Comptes Rendus Chimie | 2013 | 6 Pages |
Abstract
The acid catalysed formation of diphenylmethyl (DPM) thioethers was successfully achieved using the protic ionic liquid (pIL) triethylamine:methanesulfonic acid (TeaMs) as the reaction solvent under microwave irradiation. A slight excess of methanesulfonic acid (10% v/v) was required to facilitate the reaction, which was applied to a variety of thiols. Aliphatic, aromatic and heterocyclic aromatic thiols were converted to their corresponding DPM thioethers in high yields (63–99%), in short reaction times (5–20 min) and using mild temperatures (80–100 °C). Finally, the pIL (TeaMS) was recycled five times without loss of yield.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Luke C. Henderson, Megan T. Thornton, Nolene Byrne, Bronwyn L. Fox, Kelsey D. Waugh, Jennifer S. Squire, Linden Servinis, Joshua P. Delaney, Hannah L. Brozinski, Luke M. Andrighetto, Jarrad M. Altimari,