Abstract
Ritter reaction was carried out efficiently in subcritical water with catalytic amount of trifluoromethanesulfonic acid. The amides were formed in good to excellent yields from secondary alcohols and tert-butanol with various nitriles.
Keywords: Alcohol, amide, nitrile, ritter reaction, subcritical water, trifluoromethanesulfonic acid, chloride, boron trifluoride, sulfuric acid, silica sulfuric acid
Letters in Organic Chemistry
Title: Ritter Reaction in Subcritical Water: An Efficient and Green Method for Amides Synthesis
Volume: 9 Issue: 1
Author(s): Shengqian Jiang, Zhouyu Wang, Zhenju Jiang, Jianhui Li, Shulin Zhou and Long Pu
Affiliation:
Keywords: Alcohol, amide, nitrile, ritter reaction, subcritical water, trifluoromethanesulfonic acid, chloride, boron trifluoride, sulfuric acid, silica sulfuric acid
Abstract: Ritter reaction was carried out efficiently in subcritical water with catalytic amount of trifluoromethanesulfonic acid. The amides were formed in good to excellent yields from secondary alcohols and tert-butanol with various nitriles.
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Cite this article as:
Jiang Shengqian, Wang Zhouyu, Jiang Zhenju, Li Jianhui, Zhou Shulin and Pu Long, Ritter Reaction in Subcritical Water: An Efficient and Green Method for Amides Synthesis, Letters in Organic Chemistry 2012; 9 (1) . https://dx.doi.org/10.2174/157017812799304006
DOI https://dx.doi.org/10.2174/157017812799304006 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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