Metal-free selective synthesis of 2-substituted benzimidazoles catalyzed by Bronsted acidic ionic liquid: Convenient access to one-pot synthesis of N-alkylated 1,2-disubstituted benzimidazoles

被引:46
作者
Senapak, Warapong [1 ,2 ]
Saeeng, Rungnapha [1 ,2 ]
Jaratjaroonphong, Jaray [1 ,2 ]
Promarak, Vinich [3 ]
Sirion, Uthaiwan [1 ,2 ]
机构
[1] Burapha Univ, Fac Sci, Dept Chem, Sangsook 20131, Chonburi, Thailand
[2] Burapha Univ, Fac Sci, Ctr Excellence Innovat Chem, Sangsook 20131, Chonburi, Thailand
[3] Vidyasirimedhi Inst Sci & Technol VISTEC, Sch Mol Sci & Engn, Wangchan 21210, Rayong, Thailand
关键词
2-Substituted benzimidazole; N-Alkylated 1,2-disubstituted benzimidazole; Metal-free condition; Acidic ionic liquid; Condensation reaction; VITRO ANTIMICROBIAL ACTIVITY; LIGHT-EMITTING-DIODES; MANNICH REACTION; BENZOXAZOLE DERIVATIVES; EFFICIENT SYNTHESIS; FACILE SYNTHESIS; GREEN SYNTHESIS; PIEZOCHROMIC LUMINESCENCE; BIOLOGICAL EVALUATION; AROMATIC-COMPOUNDS;
D O I
10.1016/j.tet.2019.05.014
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A novel efficient method for the selective synthesis of 2-substituted benzimidazoles is described through condensation reaction of o-phenylenediamines with a wide rang of aliphatic, aromatic and heteroaromatic aldehyde substrates using Bronsted acidic ionic liquid as a reusable catalyst under metal-free conditions at ambient temperature. Notably, Dodecylimidazolium hydrogen sulfate ([Dodeclm][HSO4]) is the most efficient catalyst for good to excellent yields of the corresponding products (up to 98%). Subsequently, this protocol was successfully applied for the preparation of N-alkylated 1,2-disubstituted benzimidazoles in high to excellent yields via sequential one-pot reaction. In addition, catalysts are recycled at least four times without significant loss in activity. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3543 / 3552
页数:10
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