Ethanol-induced transformation of furfural into 1,4-pentanediol over a Cu/SiO2 catalyst with enhanced metal-acid sites by copper phyllosilicate

Hydrogenolysis of the large-scale biomass-derived furfural to pentanediols (PeDs) is of great significance for resource saving and development of polyester monomers. In this work, a Cu/SiO2 catalyst derived from copper phyllosilicate with enhanced metal-acid sites was developed, which demonstrated distinctive catalytic activity in the ethanol-induced conversion of furfural into 1,4-pentanediol (1,4-PeD). A significant yield of 1,4-PeD (86.2%) was obtained over the Cu/SiO2 catalyst without the addition of any solid or homogeneous acid at a mild temperature (120 degrees C). Different from the previously reported reaction routes, our work proposed a novel ethanol-induced conversion route via acid-catalyzed etherification of furfuryl alcohol and ethanol to form 2-ethoxymethyl-furan (2-(EoM)F) as the key intermediate, which followed the degradation to ethyl levulinate (EL) and hydrogenation to 1,4-PeD over metal sites. This work describes an important progress in this field by developing an efficient strategy for ethanol-induced transformation of furfural into 1,4-PeD.

Automated summary

In this study, a Cu/SiO2 catalyst derived from copper phyllosilicate was developed and demonstrated distinctive catalytic activity in the ethanol-induced conversion of furfural into 1,4-pentanediol. The proposed novel ethanol-induced conversion route involves acid-catalyzed etherification of furfuryl alcohol and ethanol, leading to the formation of 2-ethoxymethyl-furan as the key intermediate, which further undergoes degradation and hydrogenation to yield 1,4-pentanediol. This work represents an important progress in developing an efficient strategy for ethanol-induced transformation of furfural.