Abstract

N-Acetyl-D-glucosamine (NAG), the monomer of the world's second most abundant biopolymer chitin, has been for the first time converted to its corresponding amide/amino substituted sugar alcohols, smaller C2-4 polyols and N-acetylmonoethanolamine (NMEA), over noble metal catalysts in the presence of hydrogen in water. Four commercialized catalysts were investigated, and Ru/C exhibited the best performance-achieving 8.7% NMEA, 6.1% C4 polyols, and 71.9% C6 polyols (N-containing) under 180 degrees C, 40 bar H-2, 1 h with 1 mol% loading. Kinetic studies were conducted, which revealed four major reaction pathways that lead to various products. In particular, retro-aldol reaction-hydrogenation was confirmed to be the pathway forming NMEA. The effects of additives (NaOH and WO3) on the reaction were also tested.

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