DBU coupled ionic liquid-catalyzed efficient synthesis of quinazolinones from CO2 and 2-aminobenzonitriles under mild conditions. Issue 20 (25th March 2020)

• Record Type: Journal Article
• Authors: Gao, Xiang; Liu, Jiao; Liu, Zhaopeng; Zhang, Lei; Zuo, Xin; Chen, Leyuan; Bai, Xue; Bai, Qingyun; Wang, Xinlin; Zhou, Anning
• Is Part Of: RSC advances. Volume 10:Issue 20(2020)
• Page Start: 12047
• Page End: 12052
• Publication Date: 2020-03-25
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0ra00194e
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Efficient and green strategy for the chemical conversion and fixation of CO2 is an attractive topic. Abstract : Efficient and green strategy for the chemical conversion and fixation of CO2 is an attractive topic. In this work, we reported an efficient catalytic system of organic base coupled ionic liquids that could catalyse the synthesis of quinazolinones via cyclization of 2-aminobenzonitriles with CO2 under mild conditions ( e.g., 60 °C, 0.1 MPa). It was found that 1, 8-diazabicyclo[5.4.0]undec-7-ene coupled 1-butyl-3-methylimidazole acetate ionic liquids (DBU/[Bmim][OAc]) displayed excellent performance in catalysing the reactions of CO2 with 2-aminobenzonitriles, and a series of quinazolinones were obtained in high yields at atmospheric pressure. Moreover, the ILs had high stability and reusability, and can be reused at least five times without considerable decrease in catalytic activity. This protocol could also be conducted on a gram scale, and may have promising and practical applications in the production of quinazolinones.