| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1314641 | Journal of Fluorine Chemistry | 2012 | 6 Pages |
The immobilization of bis(perfluorooctanesulfonyl)imide (HNPf2) on fluorous silica gel (FSG) and its utilization in protection of carbonyls have been investigated. This system is reasonably general and can be applied to converting several carbonyls to the corresponding acetals and ketals in good to excellent yields. There is no need for the use of anhydrous solvents or inert atmosphere. Recycling studies have shown that the FSG-supported HNPf2 catalyst can be readily recovered and reused several times without significant loss of activity.
Graphical abstractThe immobilization of bis(perfluorooctanesulfonyl)imide (HNPf2) on fluorous silica gel (FSG) and its utilization in protection of carbonyls have been investigated. This system is reasonably general and can be applied to converting several carbonyls to the corresponding acetals and ketals in good to excellent yields.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Fluorous silica gel supported bis(perfluorooctanesulfonyl)imide was prepared. ► FSG–HNPf2 was characterized by FTIR, pyridine-FTIR and TGA. ► Several carbonyls was converted to acetals and ketals in good to excellent yields using FSG–HNPf2. ► FSG–HNPf2 catalyst can be easily recovered and reused several times without significant loss of activity.
