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One‐Pot Conversion of Carbon Dioxide, Ethylene Oxide, and Amines to 3‐Aryl‐2‐oxazolidinones Catalyzed with Binary Ionic Liquids
Author(s) -
Wang Binshen,
Elageed Elnazeer H. M.,
Zhang Dawei,
Yang Sijuan,
Wu Shi,
Zhang Guirong,
Gao Guohua
Publication year - 2014
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201300801
Subject(s) - ionic liquid , chemistry , catalysis , bromide , nucleophile , aryl , ethylene oxide , methyl acetate , organic chemistry , ethylene , alkyl , polymer , copolymer
An effective one‐pot method for the conversion of carbon dioxide, ethylene oxide, and amines to 3‐aryl‐2‐oxazolidinones has been developed. This one‐pot method consists of two parallel reactions and a subsequent cascade reaction between the two products of the corresponding parallel reactions. Notably, the binary ionic liquids of 1‐butyl‐3‐methyl‐imidazolium bromide and 1‐butyl‐3‐methyl‐imidazolium acetate demonstrate a synergistic catalytic effect on this new strategy. 1‐Butyl‐3‐methyl‐imidazolium bromide is essential in two parallel reactions owing to the good nucleophilicity and leaving ability of bromide, and 1‐butyl‐3‐methyl‐imidazolium acetate plays a dominant role in the subsequent cascade reaction owing to the strong basicity of acetate. In addition, the binary ionic liquids can be used thrice without significant loss of catalytic activity.