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Ionic liquids (ILs) are versatile solvents and catalysts for the synthesis of quinazoline‐2,4‐dione from 2‐aminobenzonitrile and CO2. However, the role of the IL in this reaction is poorly understood. Consequently, we investigated this reaction and showed that the IL cation does not play a significant role in the activation of the substrates, and instead plays a secondary role in controlling the physical properties of the IL. A linear relationship between the pK a of the IL anion (conjugate acid) and the reaction rate was identified with maximum catalyst efficiency observed at a pK a of >14.7 in DMSO. The base‐catalyzed reaction is limited by the acidity of the quinazoline‐2,4‐dione product, which is deprotonated by more basic catalysts, leading to the formation of the quinazolide anion (conjugate acid pK a 14.7). Neutralization of the original catalyst and formation of the quinazolide anion catalyst leads to the observed reaction limit.  相似文献   

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A novel method for the highly efficient and reversible capture of CO in carbanion‐functionalized ionic liquids (ILs) by a C‐site interaction is reported. Because of its supernucleophilicity, the carbanion in ILs could absorb CO efficiently. As a result, a relatively high absorption capacity for CO (up to 0.046 mol mol−1) was achieved under ambient conditions, compared with CO solubility in a commonly used IL [Bmim][Tf2N] (2×10−3 mol mol−1). The results of quantum mechanical calculations and spectroscopic investigation confirmed that the chemical interaction between the C‐site in the carbanion and CO resulted in the superior CO absorption capacities. Furthermore, the subsequent conversion of captured CO into valuable chemicals with good reactivity was also realized through the alkoxycarbonylation reaction under mild conditions. Highly efficient CO absorption by carbanion‐functionalized ILs provides a new way of separating and converting CO.  相似文献   

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