Synthesis of Ethyl-4-ethoxy Pentanoate by Reductive Etherification of Ethyl Levulinate in Ethanol on Pd/SiO2-C Catalysts

The synthesis of biomass-derived ethers to be used as biofuels or biofuel additives has attracted much attention. Following the recently reported synthesis of etherified ester ethyl-4-ethoxy pentanoate (EEP) from gamma-valerolactone (GVL) in ethanol catalyzed by H-beta zeolite, an alternative route to prepare EEP in high yield has been developed by reductive etherification of ethyl levulinate (EL) in ethanol at 140 degrees C under 0.5 MPa H-2 with a silica-modified Pd/C catalyst. The ether production likely follows a tandem acetalization-hydrogenolysis process with ethyl-4,4-diethoxy pentanoate (EDEP) as the intermediate. The acetalization step can be favored by introducing acidic materials, such as SiO2-carbon or beta zeolite, as a cocatalyst. The combination of the Pd/SiO2-C and beta zeolite mixture leads to 100 % EL conversion and 93 % EEP selectivity under optimized reaction conditions. For the first time, the standard molar combustion enthalpy of as-prepared EEP is measured by using a static oxygen bomb, and the value of which is determined to be about -5658 kJ mol(-1), which is much larger than that of GVL (-2650 kJ mol(-1)).