Abstract

The utilization of CO2 as a non-toxic and cheap feedstock for C1 is a desirable route to achieve high value-added chemicals. In this context, we report a highly efficient ruthenium-catalyzed semi-hydrogenation reaction of CO2 -derived ureas. Various alkyl and aryl urea derivatives were successfully hydrogenated to obtain the corresponding recyclable amines and formamides (up to 97 % yield), highlighting the good substrate applicability of this method, which makes this method a sustainable alternative for the hydrogenation of CO2 to formamides in the presence of amines. In the meantime, we have discovered a new pathway that enables rapid hydrogenation of urea derivatives even at lower H2 pressure (<5 bar). This methodology might provide a new insight into the reduction functionalization of CO2 under mild pressure to form new C-N bond. Based on the control experiments and the observed intermediate products, we clarify the mechanism for selective semi-hydrogenation of ureas.

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