Efficient synthesis of 5-ethoxymethylfurfural from biomass-derived 5-hydroxymethylfurfural over sulfonated organic polymer catalyst

• Published in: RSC advances Vol. 11; no. 6; pp. 3585 - 3595
• Main Authors: Xiang, Yanping, Wen, Sha, Tian, Yi, Zhao, Kangyu, Guo, Dongwen, Cheng, Feng, Xu, Qiong, Liu, Xianxiang, Yin, Dulin
• Format: Journal Article
• Language: English
• Published: Cambridge Royal Society of Chemistry 18.01.2021; The Royal Society of Chemistry
• Subjects: Catalysts; Catalytic activity; Catalytic converters; Chemistry; Copolymers; Divinylbenzene; Hydroxymethylfurfural; Polymers; Response surface methodology; Sulfonic acid
• ISSN: 2046-2069; 2046-2069
• DOI: 10.1039/d0ra10307a

Herein, we investigated catalytic potential of a functionalized porous organic polymer bearing sulfonic acid groups (PDVTA-SO 3 H) to the etherification of 5-hydroxymethylfurfural (HMF) to 5-ethoxymethylfurfural (EMF) under solvent-free conditions. The PDVTA-SO 3 H material was synthesized via post-synthetic sulfonation of the porous co-polymer poly-divinylbenzene- co -triallylamine by chlorosulfonic acid. The physicochemical properties of the PDVTA-SO 3 H were characterized by FT-IR, SEM, TG-DTG, and N 2 adsorption isotherm techniques. PDVTA-SO 3 H had high specific surface area (591 m 2 g −1 ) and high density of -SO 3 H group (2.1 mmol g −1 ). The reaction conditions were optimized via Box-Behnken response surface methodology. Under the optimized conditions, the PDVTA-SO 3 H catalyst exhibited efficient catalytic activity with 99.8% HMF conversion and 87.5% EMF yield within 30 min at 110 °C. The used PDVTA-SO 3 H catalyst was readily recovered by filtration and remained active in recycle runs. The sulfonic acid grafted porous organic nitrogen-containing polymer (PDVTA-SO 3 H) exhibited excellent catalytic activity in the synthesis of 5-ethoxymethylfurfural (EMF) from 5-hydroxymethylfurfural (HMF).