Synthesis of salicylates from anionically activated aromatic trifluoromethyl group
Xie H. 1Lin C. 1Wang R. 1Liu J.-B.1
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作者信息
1. Faculty of Materials Metallurgy and Chemistry Jiangxi University of Science and Technology
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Abstract
? 2021 Elsevier LtdAn efficient approach to salicylates via a novel transformation of anionically activated aromatic trifluoromethyl group is described. Anionically activated trifluoromethyl group can react with phenols/alcohols under alkaline conditions to afford aryl/alkyl salicylates in high yields. Mechanism studies indicate that the carbonyl oxygen atom of ester is from the H2O in the solvent.
Key words
2-(Trifluoromethyl)-phenol/C–F bond activation/Nucleophile/Salicylate/Trifluoromethyl group