A regioselective one-pot aza-Friedel-Crafts reaction for primary, secondary and tertiary anilines using a heterogeneous catalyst

被引:18
作者
Bosica, Giovanna [1 ]
Abdilla, Roderick [1 ]
机构
[1] Univ Malta, Dept Chem, MSD-2080 Msida, Malta
关键词
SOLVENT-FREE CONDITIONS; MANNICH-TYPE REACTION; SOLID ACID CATALYST; 3-AMINO ALKYLATED INDOLES; MULTICOMPONENT SYNTHESIS; 3-SUBSTITUTED INDOLES; CARBONYL-COMPOUNDS; AROMATIC-AMINES; EFFICIENT; 3-COMPONENT;
D O I
10.1039/c7gc02038d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A one-pot multicomponent aza-Friedel-Crafts reaction was performed under green, neat and heterogeneous conditions in the presence of 1.25 mmol% of 30% w/w silicotungstic acid supported on Amberlyst 15 beads. In a yet unprecedented attempt, both primary and secondary anilines could provide the 3-substituted indole product in good to excellent yields usually at room temperature whilst tertiary anilines gave moderate results. Interestingly all reactions proceeded regioselectively via two separate C-C bond forming reactions rather than C-C and C-N bond forming steps. The catalyst is easy, safe and environmentally-benign to prepare, completely recoverable and recyclable up to 5 times.
引用
收藏
页码:5683 / 5690
页数:8
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