A CO2-induced ROCO2Na/ROCO2H buffer solution promoted the carboxylative cyclization of propargyl alcohol to synthesize cyclic carbonates

A CO2-induced ROCO2Na/ROCO2H buffer solution is developed and employed in the carboxylative cyclization of propargyl alcohol to generate alpha-alkylene cyclic carbonates. The introduction of CO2 into the propargyl alcohol/sodium tertiary pentoxide system can provide the ROCO2Na/ROCO2H buffer solution with both basic and acidic species. The basic and acidic species can simultaneously promote the generation of a carbonate anion intermediate and the interaction between the alkyne moieties of propargyl alcohol and protons (H+), facilitating carboxylative cyclization. Furthermore, the bulky (n-C4H9)(4)N+ cation of tetrabutylammonium bromide as an additive plays a crucial role in enhancing the nucleophilicity of the carbonate anion intermediate. Various alpha-alkylene cyclic carbonates are obtained in this catalytic system with relatively good yields at 80 degrees C.