催化学报 ›› 2011, Vol. 32 ›› Issue (4): 595-598.DOI: 10.1016/S1872-2067(10)60210-0

• 研究论文 • 上一篇    下一篇

Protection of Hydroxyl Groups as a Trimethylsilyl Ether by 1,1,1,3,3,3-Hexamethyldisilazane Promoted by Aspartic Acid as an Efficient Organocatalyst

Arash GHORBANI-CHOGHAMARANI*, Masoomeh NOROUZI   

  1. Department of Chemistry, Faculty of Science, Ilam University, P.O. Box 69315516, Ilam, Iran
  • 收稿日期:2010-11-24 修回日期:2011-01-06 出版日期:2011-04-18 发布日期:2014-08-30

Protection of Hydroxyl Groups as a Trimethylsilyl Ether by 1,1,1,3,3,3-Hexamethyldisilazane Promoted by Aspartic Acid as an Efficient Organocatalyst

Arash GHORBANI-CHOGHAMARANI*, Masoomeh NOROUZI   

  1. Department of Chemistry, Faculty of Science, Ilam University, P.O. Box 69315516, Ilam, Iran
  • Received:2010-11-24 Revised:2011-01-06 Online:2011-04-18 Published:2014-08-30

摘要: A wide variety of alcohols and phenols were protected as trimethylsilyl ethers using 1,1,1,3,3,3-hexamethyl disilazane catalyzed by aspartic acid as a non-toxic, metal-free, and green organocatalyst at room temperature in acetonitrile under mild and heterogeneous conditions. The procedure is operationally simple and the silylated product was obtained in high yield and purity.

关键词: alcohol, phenol, 1,1,1,3,3,3-hexamethyldisilazane, trimethylsilylation, protection

Abstract: A wide variety of alcohols and phenols were protected as trimethylsilyl ethers using 1,1,1,3,3,3-hexamethyl disilazane catalyzed by aspartic acid as a non-toxic, metal-free, and green organocatalyst at room temperature in acetonitrile under mild and heterogeneous conditions. The procedure is operationally simple and the silylated product was obtained in high yield and purity.

Key words: alcohol, phenol, 1,1,1,3,3,3-hexamethyldisilazane, trimethylsilylation, protection