2014Green Chemistry Letters and ReviewsOpen access

Long-chain double SO3H-functionalized Brønsted acidic ionic liquids catalyzed selective alkylation of phenol andp-cresol with tert-butanol

Xinzhong Li, Rong Cao, Qi Lin

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Abstract

A simple, efficient, and selective approach for the tert-butylation of phenol and p-cresol using two double SO3H-functionalized long-chain Brønsted acidic ionic liquids as recyclable catalysts is reported. Under optimum reaction conditions, 89.4% conversion of the phenol and 73.7% selectivity of 2,4-tert-butyl-phenol and 93.2% conversion of the p-cresol and 89.2% selectivity of 2-tert-butyl-p-cresol were obtained. Two ionic liquids could be recovered readily and their catalytic activity almost completely retained after five recycles.

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A simple, efficient, and selective approach for the tert-butylation of phenol and p-cresol using two double SO3H-functionalized long-chain Brønsted acidic ionic liquids as recyclable catalysts is reported. Under optimum reaction conditions, 89.4% conversion of the phenol and 73.7% selectivity of 2,4-tert-butyl-phenol and 93.2% conversion of the p-cresol and 89.2% selectivity of 2-tert-butyl-p-cresol were obtained. Two ionic liquids could be recovered readily and their catalytic activity almost completely retained after five recycles.

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Available abstract

A simple, efficient, and selective approach for the tert-butylation of phenol and p-cresol using two double SO3H-functionalized long-chain Brønsted acidic ionic liquids as recyclable catalysts is reported. Under optimum reaction conditions, 89.4% conversion of the phenol and 73.7% selectivity of 2,4-tert-butyl-phenol and 93.2% conversion of the p-cresol and 89.2% selectivity of 2-tert-butyl-p-cresol were obtained. Two ionic liquids could be recovered readily and their catalytic activity almost completely retained after five recycles.

Key concepts: Chemistry, Phenol, p-Cresol, Selectivity, Catalysis, Alkylation, Ionic liquid, Cresol

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