MOF-catalyzed hydroxyalkylation-alkylation reaction for the controlled synthesis of furan oligomers

被引:10
作者
Atayde Jr, Eduardo C. [1 ,2 ,3 ]
Matsagar, Babasaheb M. [3 ]
Wang, Yu-Cheng [3 ]
Wu, Kevin C. -W. [1 ,3 ,4 ]
机构
[1] Acad Sinica, Mol Sci & Technol Program, Taiwan Int Grad Program, 128,Sec 2,Acad Rd, Taipei 11529, Taiwan
[2] Natl Tsing Hua Univ, Dept Chem, 101,Sec 2,Kuang Fu Rd, Hsinchu 30013, Taiwan
[3] Natl Taiwan Univ, Dept Chem Engn, 1,Sec 2,Roosevelt Rd, Taipei 10617, Taiwan
[4] Yuan Ze Univ, Dept Chem Engn & Mat Sci, Taoyuan, Taiwan
关键词
Biomass; Catalysis; Furan oligomers; Hydroxylalkylation/alkylation reactions; Metal-organic frameworks; DIESEL-RANGE ALKANES; HIGH-QUALITY DIESEL; SELECTIVE PRODUCTION; FUEL PRECURSORS; ACID CATALYSTS; 2-METHYLFURAN; CARBON; HYDRODEOXYGENATION; CONDENSATION; DERIVATIVES;
D O I
10.1016/j.apcata.2023.119492
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydroxyalkylation-alkylation (HAA) reaction is a type of C-C coupling technique utilized in the production of furan oligomers, which are potential biofuel precursors. In this study, we present the first application of an acidic MOF, Sulfated MOF-808, in catalyzing the HAA reactions of a series of furan oligomers with high yield and selectivity. Specifically, we focused on the optimization of the HAA between 5-methylfurfural (5-MFUR) and 2methylfuran (2-MF) by varying different reaction conditions, which afforded a quantitative yield reaching 97% while preventing the self-condensation of 2-MF. The catalyst was also found to be recyclable and can be reused without significant loss in its activity. Lastly, we extended the substrate scope to include benzene-based electrophiles, thereby further proving the versatility of the Sulfated MOF-808 catalyst in the HAA reactions of a variety of starting materials.
引用
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页数:9
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