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One-Step Conversion of Biomass-Derived Furanics into Aromatics by Bronsted Acid Ionic Liquids at Room Temperature
Ni, Lingli1,2; Xin, Jiayu1; Jiang, Kun1; Chen, Lu1,2; Yan, Dongxia1; Lu, Xingmei1; Zhang, Suojiang1
2018-02-01
Source PublicationACS SUSTAINABLE CHEMISTRY & ENGINEERING
ISSN2168-0485
Volume6Issue:2Pages:2541-2551
AbstractAromatics play essential and unique roles in the areas ranging from synthetic chemistry to the manufacturing industry. Production of aromatics from biomass is of great fundamental interest and practical importance to ease the burden of fossil resources. This work delineates a one-step route for the synthesis of renewable aromatics from various biobased furanics and dienophiles by acidic ionic liquids at mild conditions. [Bmim]HSO4 was used as a catalyst and solvent for the direct conversion of 2,5-dimethylfuran and acrylic acid into p-xylene and 2,5-dimethylbenzoic acid; up to 89% aromatic selectivity was achieved at 87% conversion of 2,5-dimethylfuran at room temperature and atmospheric pressure, and totally 84% selectivity of p-xylene can be obtained with a subsequent decarboxylation reaction. The reaction mechanism study supplemented with isotopic tracing and DFT calculations revealed the lowest-energy pathway for the two main products. Various starting materials were studied for further extensions of the method, and it turned out that electron-donating methyl groups on the furan ring played crucial roles on the activation of dehydration and decarboxylation processes. This work provided convenient access to industrial commodity aromatics from fully biomass-derived feedstocks and thus can be regarded more economically and environmentally feasible.
KeywordBiomass Cycloaddition Acidic Ionic Liquid Aromatics
SubtypeArticle
WOS HeadingsScience & Technology ; Physical Sciences ; Technology
DOI10.1021/acssuschemeng.7b04017
Indexed BySCI
Language英语
WOS KeywordDIELS-ALDER CYCLOADDITION ; RENEWABLE P-XYLENE ; ACRYLIC-ACID ; CARBOXYLIC-ACIDS ; CATALYZED PROTODECARBOXYLATION ; DEHYDRATION REACTIONS ; BIOBASED FURANICS ; BENZOIC-ACID ; ETHYLENE ; ZEOLITES
WOS Research AreaChemistry ; Science & Technology - Other Topics ; Engineering
WOS SubjectChemistry, Multidisciplinary ; GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY ; Engineering, Chemical
Funding OrganizationNational Basic Research Program of China (973 Program)(2015CB251401) ; National Natural Science Foundation of China(21576269 ; 21210006 ; 21476245 ; 21406230)
WOS IDWOS:000424728300110
Citation statistics
Cited Times:3[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.ipe.ac.cn/handle/122111/24014
Collection多相复杂系统国家重点实验室
Affiliation1.Chinese Acad Sci, Inst Proc Engn, State Key Lab Multiphase Complex Syst, Beijing Key Lab Ion Liquids Clean Proc,Key Lab Gr, 1 North Second St, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Sino Danish Coll, 380 Huaibeizhuang, Beijing 101408, Peoples R China
Recommended Citation
GB/T 7714
Ni, Lingli,Xin, Jiayu,Jiang, Kun,et al. One-Step Conversion of Biomass-Derived Furanics into Aromatics by Bronsted Acid Ionic Liquids at Room Temperature[J]. ACS SUSTAINABLE CHEMISTRY & ENGINEERING,2018,6(2):2541-2551.
APA Ni, Lingli.,Xin, Jiayu.,Jiang, Kun.,Chen, Lu.,Yan, Dongxia.,...&Zhang, Suojiang.(2018).One-Step Conversion of Biomass-Derived Furanics into Aromatics by Bronsted Acid Ionic Liquids at Room Temperature.ACS SUSTAINABLE CHEMISTRY & ENGINEERING,6(2),2541-2551.
MLA Ni, Lingli,et al."One-Step Conversion of Biomass-Derived Furanics into Aromatics by Bronsted Acid Ionic Liquids at Room Temperature".ACS SUSTAINABLE CHEMISTRY & ENGINEERING 6.2(2018):2541-2551.
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