Ambient-pressure alkoxycarbonylation for sustainable synthesis of ester
Bin Zhang, Haiyang Yuan, Ye Liu, Zijie Deng, Mark Douthwaite, Nicholas F. Dummer, Richard J. Lewis, Xingwu Liu, Sen Luan, Minghua Dong, Tianjiao Wang, Qingling Xu, Zhijuan Zhao, Huizhen Liu, Buxing Han, Graham J. Hutchings
Abstract
Abstract Alkoxycarbonylation reactions are common in the chemical industry, yet process sustainability is limited by the inefficient utilization of CO. In this study, we address this issue and demonstrate that significant improvements can be achieved by adopting a heterogeneously catalyzed process, using a Ru/NbO x catalyst. The Ru/NbO x catalyst enables the direct synthesis of methyl propionate, a key industrial commodity, with over 98% selectivity from CO, ethylene and methanol, without any ligands or acid/base promoters. Under ambient CO pressure, a high CO utilization efficiency (336 mmol ester mol CO −1 h −1 ) is achieved. Mechanistic investigations reveal that CO undergoes a methoxycarbonyl (COOCH 3 ) intermediate pathway, attacking the terminal carbon atom of alkene and yielding linear esters. The origins of prevailing linear regioselectivity in esters are revealed. The infrared spectroscopic feature of the key COOCH 3 species is observed at 1750 cm −1 (C=O vibration) both experimentally and computationally. The broad substrate applicability of Ru/NbO x catalyst for ester production is demonstrated. This process offers a sustainable and efficient approach with high CO utilization and atom economy for the synthesis of esters.