The Transesterification of Dimethyl Carbonate with Phenol over Mg−Al-hydrotalcite Catalyst
Mei Fuming, Pei Zhi, LI Guang-xing
Abstract
Mei Fuming, Pei Zhi, LI Guang-xing
Abstract
The production of diphenyl carbonate (DPC) by the transesterification of dimethyl carbonate (DMC) with phenol was performed using a variety of solid catalysts. Mg−Al-hydrotalcite was found to have a high activity for this transesterification. A 14.7% yield of DPC and an 11.6% yield of methylphenyl carbonate (MPC) based on DMC were obtained in the presence of Mg−Al-hydrotalcite catalyst. The optimum experimental temperature for this transesterification reaction was between 160 and 180 °C, which was in agreement with the thermodynamic analysis. When the transesterification of DMC with phenol was performed at the molar ratio of phenol to DMC of 2:1, reaction time 10 h, 1.0% of 2:1 Mg−Al-hydrotalcite based on the total weight of reactants, and 160−180 °C, the total yield and selectivity for DPC and MPC were 26.3 and 82.4%, respectively. The yield of anisole was 5.6%.
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The production of diphenyl carbonate (DPC) by the transesterification of dimethyl carbonate (DMC) with phenol was performed using a variety of solid catalysts. Mg−Al-hydrotalcite was found to have a high activity for this transesterification. A 14.7% yield of DPC and an 11.6% yield of methylphenyl carbonate (MPC) based on DMC were obtained in the presence of Mg−Al-hydrotalcite catalyst. The optimum experimental temperature for this transesterification reaction was between 160 and 180 °C, which was in agreement with the thermodynamic analysis. When the transesterification of DMC with phenol was performed at the molar ratio of phenol to DMC of 2:1, reaction time 10 h, 1.0% of 2:1 Mg−Al-hydrotalcite based on the total weight of reactants, and 160−180 °C, the total yield and selectivity for DPC and MPC were 26.3 and 82.4%, respectively. The yield of anisole was 5.6%.
Key concepts: Transesterification, Dimethyl carbonate, Hydrotalcite, Diphenyl carbonate, Chemistry, Anisole, Catalysis, Phenol