1,3-Bis(carboxymethyl)imidazolium Chloride as a Metal-Free and Recyclable Catalyst for the Synthesis of N-Allylanilines by Allylic Substitution of Alcohols

被引:21
作者
Albert-Soriano, Maria
Hernandez-Martinez, Laura
Pastor, Isidro M. [1 ]
机构
[1] Univ Alicante, Organ Chem Dept, Apdo 99, E-03080 Alicante, Spain
关键词
Imidazolium salt; Allylic substitution; Metal-free; Allylic anilines; Sustainable; DIRECT AMINATION; NUCLEOPHILIC-SUBSTITUTION; IONIC LIQUIDS; HYDROXY GROUP; GRAPHENE OXIDE; IMIDAZOLIUM; PALLADIUM; AMINES; ALKYLATION; ALLYLATION;
D O I
10.1021/acssuschemeng.8b02614
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The 1,3-bis(carboxymethyl)imidazolium chloride, which is easily and in a straightforward manner prepared readily from starting materials in multigram scale, is employed as catalyst in the synthesis of N-allylanilines by allylic substitution of alcohols with anilines. This metal-free catalyst allows the reaction to be carried out under mild reaction conditions (80 degrees C and air open vessel) and proved to be efficient for a diversity of anilines and allylic alcohols, providing exclusively the product of N-substitution independently of the substituents in the aniline reactant. The process described is simple and effective, allowing N-allylanilines to be obtained in preparative scale [e.g., 3.30 g of N-(1,3diphenylallyl)-4-nitroaniline]. The catalyst could be reused up to 15 cycles without loss of activity, proving its robustness.
引用
收藏
页码:14063 / 14070
页数:15
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