Glycidol: an Hydroxyl-Containing Epoxide Playing the Double Role of Substrate and Catalyst for CO2 Cycloaddition Reactions

Glycidol is converted into glycerol carbonate (GC) by coupling with CO2 in the presence of tetrabutylammonium bromide (TBAB) under mild reaction conditions (T=60 °C, PCO2 =1 MPa) in excellent yields (99 %) and short reaction time (t=3 h). The unusual reactivity of this substrate compared to other epoxides, such as propylene oxide, under the same reaction conditions is clearly related to the presence of a hydroxyl functionality on the oxirane ring. Density functional theory calculations (DFT) supported by 1H NMR experiments reveal that the unique behavior of this substrate is a result of the formation of intermolecular hydrogen bonds into a dimeric structure, activating this molecule to nucleophilic attack, and allowing the formation of GC. Furthermore, the glycidol/TBAB catalytic system acts as an efficient organocatalyst for the cycloaddition of CO2 to various oxiranes. Double duty: Glycydol is efficiently converted to glycerol carbonate by coupling with CO2 in the presence of tetrabutylammonium bromide under metal‐free, solvent free reaction conditions. Density functional theory calculations supported by 1H NMR experiments reveal that the unique behavior of this substrate is a result of the formation of intermolecular hydrogen bonds, activating this molecule to nucleophilic attack.