Probing the mechanism of baylis-hillman reaction in ionic liquids

TitleProbing the mechanism of baylis-hillman reaction in ionic liquids
Publication TypeJournal Article
Year of Publication2012
AuthorsSingh, A, Kumar, A
JournalJournal of Organic Chemistry
Volume77
Issue19
Pagination8775-8779
Date PublishedOCT
ISSN0022-3263
Abstract

The kinetic data for a Baylis-Hillman reaction in certain ionic liquids possessing ethylsulfate anion [EtSO4](-) demonstrate that the rate determining step (RIDS) is second order in aldehyde, but first order in acrylate and DABCO. This observation is similar to the one made by McQuade et al., who carried out this reaction in an aprotic polar solvent like DMSO. However, this is in contrast to the general observation that ADS is first order in aldehyde, acrylate, and DABCO in organic solvents.

DOI10.1021/jo301348k
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)4.564
Divison category: 
Physical and Materials Chemistry