N-Acyl DBN Tetraphenylborate Salts as N-Acylating Agents

被引:29
|
作者
Taylor, James E. [1 ]
Jones, Matthew D. [1 ]
Williams, Jonathan M. J. [1 ]
Bull, Steven D. [1 ]
机构
[1] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
来源
JOURNAL OF ORGANIC CHEMISTRY | 2012年 / 77卷 / 06期
关键词
AMIDE BOND FORMATION; CARBOXYLIC-ACIDS; BORROWING HYDROGEN; EFFICIENT; REAGENTS; SULFONAMIDES; ALCOHOLS; AMINES; MILD; ACYLBENZOTRIAZOLES;
D O I
10.1021/jo202647f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Air-stable and crystalline N-acyl DBN tetraphenylborate salts have been synthesized from 1,5-diazabicyclo[4.3.0]non-5-ene (DBN) and the corresponding acyl chloride in the presence of sodium tetraphenylborate. The salts have been shown to be effective N-acylating agerets, reacting with primary amines, secondary amines, and sulfonamides to form the corresponding N-acylated products in good yields. The DBN hydrotetraphenylborate byproduct can be conveniently removed by filtration, providing pure N-acylated products without the need for further purification. The N-acyl DBN tetraphenylborate salts are attractive alternatives to acyl halides as they can be stored in air without decomposition, avoid the production of free acid during acylation reactions, and can be used under more forcing thermal conditions.
引用
收藏
页码:2808 / 2818
页数:11
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