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Sulfonic Acid-Functionalized Ionic Liquids as Metal-Free, Efficient and Reusable Catalysts for Direct Amination of Alcohols
被引:60
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.
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页码:1052 / 1060
页数:9
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