| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 68571 | Journal of Molecular Catalysis A: Chemical | 2006 | 6 Pages |
Perchloric acid immobilized on silica gel has been found to be an efficient and expedient catalyst for geminal diacylation of aldehydes. A wide variety of aromatic and aliphatic aldehydes can be easily transformed into the corresponding acylals using 0.5 mol% HClO4-SiO2 within 2–10 min under solvent-free conditions at room temperature. The notable advantages of this protocol are: the reaction requires less reaction time and only stoichiometric amount of acetic anhydride being used, is highly economic and the catalyst is recyclable.
Graphical abstractSilica supported perchloric acid (HClO4-SiO2): A highly efficient and reusable catalyst for geminal diacylation of aldehydes under solvent-free conditions. Figure optionsDownload full-size imageDownload as PowerPoint slide
