Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5267334 | Tetrahedron Letters | 2015 | 20 Pages |
Abstract
A method for the bromination of alkoxy-substituted benzenes and naphthalenes was developed by using the residual oxygen in the reaction tube as the oxidant, and [Bmim]NO3 (1-butyl-3-methylimidazolium nitrate) ionic liquid as both the catalyst and solvent. No other reagent apart from the ionic liquid and molecular bromine was used in the reactions, and basically all the bromine atoms in bromine source were transferred to the bromination products, showing that the presented protocol is highly atom economic and clean.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yun-Lai Ren, Binyu Wang, Xin-Zhe Tian, Shuang Zhao, Jianji Wang,