Alcohol amine-catalyzed CO2 conversion for the synthesis of quinazoline-2, 4-(1H, 3H)-dione in water. Issue 57 (21st September 2020)

• Record Type: Journal Article
• Authors: Sheng, Zhi-Zheng; Huang, Min-Min; Xue, Teng; Xia, Fei; Wu, Hai-Hong
• Is Part Of: RSC advances. Volume 10:Issue 57(2020)
• Page Start: 34910
• Page End: 34915
• Publication Date: 2020-09-21
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0ra06439d
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Commercial DEA is proposed for efficiently promoting the cyclization of CO2 and 2-aminobenzonitrile to quinazoline-2, 4(1 H, 3 H )-dione (up to 94% yield) while water acts as the solvent and co-catalyst. Abstract : The conversion of CO2 to high value-added chemicals in water using environment-friendly and cost-effective catalysts is a very significant topic. In this work, a green method for the conversion of CO2 catalyzed by alcohol amines has been developed. Alcohol amines showed considerable activating ability to CO2 in the cyclization with 2-aminobenzonitrile to quinazoline-2, 4(1 H, 3 H )-dione in water. Notably, when diethanolamine (DEA) was used as the catalyst, 94% yield of quinazoline-2, 4-(1 H, 3 H )-dione could be achieved. A plausible mechanism has been proposed based on the 1 H NMR, FT-IR analysis and DFT calculation. The excellent catalytic performance is attributed to the combined effect of both the secondary amine and hydroxyl groups on alcohol amines with the assistance of water in the formation of carbamate. Water plays a bi-functional role of solvent and co-catalyst in this catalytic process. Catalysts can be easily recovered and reused five times without significant loss of activity.