Sulfonic Acid-Functionalized Ionic Liquids as Metal-Free, Efficient and Reusable Catalysts for Direct Amination of Alcohols

被引:59
|
作者
Han, Feng [1 ,2 ]
Yang, Lei [1 ]
Li, Zhen [1 ]
Xia, Chungu [1 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
基金
美国国家科学基金会;
关键词
alcohols; amination; ionic liquids; sulfonic acid-functionalized ionic liquids; NUCLEOPHILIC-SUBSTITUTION; BENZYL ALCOHOLS; HYDROXY GROUP; N-ALKYLATION; ALLYLIC ALCOHOLS; SULFONAMIDES; ARYLATION; SOLVENT; MONTMORILLONITE; TOSYLARYLIMINES;
D O I
10.1002/adsc.201100886
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of sulfonic acid-functionalized (SO3H-functionalized) ionic liquids was synthesized and used as metal-free, highly selective and efficient catalysts for the direct amination of alcohols. Notably, the activities of the series of SO3H-functionalized ionic liquids were compared and a 92% isolated yield was obtained using 3-tetradecyl-1-(butyl-4- sulfonyl)imidazolium trifluoromethanesulfonate ([BsTdIM][OTf]) as the catalyst. Importantly, the catalytic system has wide substrate scope including benzylic, allyl, propargylic, aliphatic alcohols with sulfonamide, amide, carbamate, aromatic amine and N-heterocyclic compounds. Interestingly, the system was also suitable for a multi-gram scale direct amination of alcohols. Additionally, the reusable nature of [BsTdIM][OTf] makes this protocol more attractive and avoids the disposal and neutralization of acidic catalysts. Moreover, preliminary experiments indicated that this reaction should proceed via an SN1 pathway.
引用
收藏
页码:1052 / 1060
页数:9
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