Paper
p-Toluenesulfonyl Chloride (p-TsCl)-Catalyzed Trimethylsilylation of Hydroxyl Groups Using Hexamethyldisilazane and Their Regeneration Under Mild Conditions: The First Example for Catalytic Application of p-Toluenesulfonyl Chloride
Published Sep 4, 2009 · A. Khazaei, A. Rostami, Fatemeh Mantashlo
Phosphorus, Sulfur, and Silicon and the Related Elements
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Abstract
The first catalytic application of p-toluenesulfonyl chloride (p-TsCl) for the efficient and selective trimethylsilylation of various types of hydroxyl groups with hexamethyldisilazane (HMDS) in dichloromethane and desilylation of these compounds in water is reported. The reactions were carried out at room temperature and were found to proceed in good to excellent yields.
p-toluenesulfonyl chloride catalyzes efficient and selective trimethylsilylation of various hydroxyl groups with hexamethyldisilazane in dichloromethane, leading to good to excellent yields and mild conditions for desilylation.
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