Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
59648 | Chinese Journal of Catalysis | 2008 | 5 Pages |
Abstract
Aromatic and aliphatic aldehydes were transformed to 1,1-diacetates (acylals) under mild conditions by treatment with acetic anhydride and Cu3/2PMo12O40/SiO2 catalyst. This catalyst was efficient for the preparation of 1,1-diacetate under solvent-free conditions. The reverse reaction using the resulting 1,1-diacetate was achieved using the same catalyst in acetonitrile as a solvent. This new method has the advantages of excellent yields and short reaction time. The catalyst can be reused several times although it gets less active.
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