One-flow syntheses of diverse heterocyclic furan chemicals directly from fructose via tandem transformation platform

被引:46
作者
Jeong, Guan-Young [1 ]
Singh, Ajay K. [1 ]
Sharma, Siddharth [2 ]
Gyak, Ki Won [1 ]
Maurya, Ram Awatar [3 ]
Kim, Dong-Pyo [1 ]
机构
[1] POSTECH Pohang Univ Sci & Technol, Natl Ctr Appl Microfluid Chem, Dept Chem Engn, Pohang 790784, South Korea
[2] Guru Nanak Dev Univ, Dept Chem, Amritsar, Punjab, India
[3] Indian Inst Chem Technol, CSIR, Div Nat Prod Chem, Hyderabad 500007, Andhra Pradesh, India
基金
新加坡国家研究基金会;
关键词
ONE-POT SYNTHESIS; CATALYTIC CONVERSION; EFFICIENT PRODUCTION; 2,5-DIFORMYLFURAN; BIOMASS; MICROREACTOR; ACID; DECARBONYLATION; CHEMISTRY; FUELS;
D O I
10.1038/am.2015.21
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The sustainable green chemistry associated with lignocellulosic biomass is of current interest for producing various chemical feedstocks via multi-step transformation processes. Here we introduce a chemical platform system for the multicomponent cascade transformation of natural lignocellulosic biomass resources. We demonstrate the concept by developing an integrated continuous two-step microfluidic system as a tandem transformation platform for direct conversion of fructose to diverse furan chemicals with excellent yields up to 99% via decarbonylation, etherification, oxidation and hydrogenolysis of a 5-hydroxymethylfurfural (HMF) intermediate. A sequential two-step process is utilized to complete the dehydration of fructose in the surface acid catalyst at 150 degrees C for 6 min, which is followed by the four types of HMF conversion in a binary or ternary phase to produce furfuryl alcohol (94% yield), 5-ethoxymethylfurfural (99%), 2,5-diformylfuran (82%) and 2,5-dimethylfuran (90%) with magnetic-based heterogeneous catalysts at 70-150 degrees C for 6-60 min. This innovative tandem microfluidic platform enables precise control of the reaction temperature and time for each individual biomass conversion step in a one-flow manner with no separation and purification steps for intermediates and catalysts.
引用
收藏
页码:e173 / e173
页数:8
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