Affiliation:
1. Department of Chemistry ZJU-NHU United R&D Center Zhejiang University Hangzhou 310027 China
2. State Key Laboratory of Chemical Engineering College of Chemical and Biological Engineering Zhejiang University Hangzhou 310027 China
Abstract
AbstractThe utilization of CO2as 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 CO2to 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 H2pressure (<5 bar). This methodology might provide a new insight into the reduction functionalization of CO2under 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.
Funder
National Key Research and Development Program of China
Natural Science Foundation of Zhejiang Province
Fundamental Research Funds for the Central Universities
National Natural Science Foundation of China
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
5 articles.
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