Hydroesterification of tert-butyl alcohol in room temperature ionic liquids

Abstract

Hydroesterification of tert-butyl alcohol with ethanol catalyzed by transition metal triphenylphosphine complexes in the presence of p-toluenesulfonic acid was investigated using room temperature ionic liquids as the reaction medium at 373–413 K and 3–6 MPa of CO. In comparison with the organic solvents as reaction medium, higher conversion was achieved and ethyl tert-valerate could be directly formed in the ionic liquid medium. The products could be separated from the ionic liquids easily due to their immiscibility in this medium.