Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1315570 | Journal of Fluorine Chemistry | 2007 | 6 Pages |
Abstract
In fluorous biphase system, hafnium(IV) bis(perfluorooctanesulfonyl)amide complex (Hf[N(SO2C8F17)2]4) was found to be a highly reactive and recyclable Lewis acid catalyst for Friedel–Crafts acylation and Prins reaction at significantly low catalyst loadings (≤1 mol%). In these reactions, Hf[N(SO2C8F17)2]4 is selectively soluble in the lower fluorous phase and can be recovered simply by phase separation. Furthermore, the catalyst can be reused without decrease of activity.
Graphical abstractAt low catalyst loadings (≤1 mol%), fluorous biphase Hf[N(SO2C8F17)2]4 Lewis acid catalyst can work efficiently for Friedel–Crafts acylation and Prins reaction. Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Xiuhua Hao, Akihiro Yoshida, Nobuto Hoshi,