Abstract
Alkyl cyanides are prepared in good to excellent yields (average yield 93% )by treatment of alcohols and thiols with 2,4,6-trichloro[1,3,5]triazine/n-Bu4NCN in refluxing acetonitrile. This method is highly selective for conversion of 1° alcohols in the presence of 2° and 3° ones and thiols.
Keywords: 2,4,6-Trichloro[1,3,5] triazine(TT), alcohol, thiol, alkyl cyanide
Letters in Organic Chemistry
Title: A New and Convenient Method of Generating Alkyl Cyanides from Alcohols and Thiols Using 2,4,6-Trichloro[1,3,5]Triazine/n-Bu4NCN
Volume: 2 Issue: 8
Author(s): Batool Akhlaghinia and Elham Roohi
Affiliation:
Keywords: 2,4,6-Trichloro[1,3,5] triazine(TT), alcohol, thiol, alkyl cyanide
Abstract: Alkyl cyanides are prepared in good to excellent yields (average yield 93% )by treatment of alcohols and thiols with 2,4,6-trichloro[1,3,5]triazine/n-Bu4NCN in refluxing acetonitrile. This method is highly selective for conversion of 1° alcohols in the presence of 2° and 3° ones and thiols.
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Cite this article as:
Akhlaghinia Batool and Roohi Elham, A New and Convenient Method of Generating Alkyl Cyanides from Alcohols and Thiols Using 2,4,6-Trichloro[1,3,5]Triazine/n-Bu4NCN, Letters in Organic Chemistry 2005; 2 (8) . https://dx.doi.org/10.2174/157017805774717571
DOI https://dx.doi.org/10.2174/157017805774717571 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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