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1-Hydroxyethyl-2-substituted phenoxymethyl benzimidazoles: synthesis and crystal structures.
Author(s)
Jiacheng Wu Key Laboratory of Leather Chemistry and Engineering of Ministry of Education, Sichuan University, Chengdu, China; National Engineering Laboratory for Clean Technology of Leather Manufacture, Sichuan University, Chengdu, China
Li Zhao Key Laboratory of Leather Chemistry and Engineering of Ministry of Education, Sichuan University, Chengdu, China;National Engineering Laboratory for Clean Technology of Leather Manufacture, Sichuan University, Chengdu, China
Changqing Zhao College of Bioengineering, Sichuan University of Science and Engineering, Zigong, China
Zhiyuan Wang Key Laboratory of Leather Chemistry and Engineering of Ministry of Education, Sichuan University, Chengdu, China;National Engineering Laboratory for Clean Technology of Leather Manufacture, Sichuan University, Chengdu, China
Haibin Gu Key Laboratory of Leather Chemistry and Engineering of Ministry of Education, Sichuan University, Chengdu, China; National Engineering Laboratory for Clean Technology of Leather Manufacture, Sichuan University, Chengdu, China
Wuyong Chen Key Laboratory of Leather Chemistry and Engineering of Ministry of Education, Sichuan University, Chengdu, China; National Engineering Laboratory for Clean Technology of Leather Manufacture, Sichuan University, Chengdu, China
Abstract
Five novel 1-hydroxyethyl-2-substituted phenoxymethyl benzimidazoles c1-c5 were successfully synthesized by a three-step route. Firstly, five substituted phenoxymethyl acids a1-a5 were prepared by the O-carboxymethylation reaction of the starting substituted phenols under microwave irradiation. Then, these compounds reacted with o-phenylendiamine to get the key intermediates 2-substituted phenoxymethyl benzimidazoles b1-b5. At last, the target compounds were synthesized by the N-hydroxyethylation reaction of b1-b5 with 2-chloroethyl alcohol through the solid-liquid phase transfer catalysis method, where tetrabutyl ammonium bromide (TBAB) was used as the catalyst. The structures of the target compounds were well characterized and verified by elemental analysis, MS, IR, 1H NMR, 13C NMR and single crystal X-ray diffraction analysis.
Publication Details
Page(s) 307-312
DOI DOI not available
Published Journal: Journal of Chemical Society of Pakistan, Volume: 38, Issue: 2, Year: 2016
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