Synthesis of furfural from xylose using a choline chloride-based deep eutectic solvent and mechanistic insights

被引:3
作者
Delgadillo, Daniela Margarita Echeverri [1 ]
Castro, Gabriel Abranches Dias [1 ]
Fernandes, Sergio Antonio [1 ]
机构
[1] Univ Fed Vicosa, Dept Quim, Grp Quim Supramol & Biomimet GQSB, CCE, BR-36570900 Vicosa, MG, Brazil
关键词
CONVERSION; ACID; CATALYST; XYLAN; ORGANOCATALYST; CHEMISTRY; DEPLETION;
D O I
10.1039/d3re00547j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The exacerbated use of fossil resources, along with the fact that these materials are raw materials from a non-renewable source, has caused a worldwide concern for their replacement. In view of this, biomass is identified as the best renewable raw material option to replace these materials in the production of energy, fuels and chemical products. Among the substances that can be obtained from biomass, furfural as a platform molecule deserves to be highlighted as it can facilitate the access of numerous substances useful for the society. Therefore, in this study, a green methodology was developed for the synthesis of furfural. For this, a biphasic system was used, where the reaction phase consisted of an acid deep eutectic solvent (DES) based on choline chloride ([Ch]Cl), water, p-toluenesulfonic acid (PTSA) and xylose and the extractor phase consisted of ethyl acetate. Using this system, it was possible to obtain furfural with a yield of 50% by heating the mixture at 130 degrees C for 15 min in a microwave reactor. Finally, the results presented were promising, with potential as a basis for the development of methods for the synthesis of furfural in biorefineries using DES, and, in addition, a discussion is carried out on the mechanistic route that leads to the formation of furfural. Choline chloride-based deep eutectic solvents can be used in the green synthesis of furfural, a platform molecule derived from biomass.
引用
收藏
页码:1560 / 1568
页数:9
相关论文
共 51 条
  • [1] Deep eutectic solvents formed between choline chloride and carboxylic acids: Versatile alternatives to ionic liquids
    Abbott, AP
    Boothby, D
    Capper, G
    Davies, DL
    Rasheed, RK
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (29) : 9142 - 9147
  • [2] Novel solvent properties of choline chloride/urea mixtures
    Abbott, AP
    Capper, G
    Davies, DL
    Rasheed, RK
    Tambyrajah, V
    [J]. CHEMICAL COMMUNICATIONS, 2003, (01) : 70 - 71
  • [3] pH-Controlled Efficient Conversion of Hemicellulose to Furfural Using Choline-Based Deep Eutectic Solvents as Catalysts
    Arora, Shalini
    Gupta, Neeraj
    Singh, Vasundhara
    [J]. CHEMSUSCHEM, 2021, 14 (18) : 3953 - 3958
  • [4] ENVIRONMENTAL-DAMAGE DUE TO FOSSIL-FUELS USE
    BARBIR, F
    VEZIROGLU, TN
    PLASS, HJ
    [J]. INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 1990, 15 (10) : 739 - 749
  • [5] Fossil fuel depletion and socio-economic scenarios: An integrated approach
    Capellan-Perez, Inigo
    Mediavilla, Margarita
    de Castro, Carlos
    Carpintero, Oscar
    Javier Miguel, Luis
    [J]. ENERGY, 2014, 77 : 641 - 666
  • [6] Castro GAD, 2023, REACT CHEM ENG, V8, P1969, DOI [10.1039/d3re00017f, 10.1039/D3RE00017F]
  • [7] Green synthesis of 5-hydroxymethylfurfural and 5-acetoxymethylfurfural using a deep eutectic solvent in a biphasic system assisted by microwaves
    Castro, Gabriel Abranches Dias
    Fernandes, Sergio Antonio
    de Sousa, Rita de Cassia Superbi
    Pereira, Matheus Mendonca
    [J]. REACTION CHEMISTRY & ENGINEERING, 2023, 8 (06) : 1324 - 1333
  • [8] Sustainable synthesis of acetals from glycerol as potential additives for biofuels under solvent-free conditions
    Castro, Gabriel Abranches Dias
    Santos, Ana Luiza Quintao
    Sathicq, angel Gabriel
    Palermo, Valeria
    Romanelli, Gustavo Pablo
    Fernandes, Sergio Antonio
    [J]. REACTION CHEMISTRY & ENGINEERING, 2022, 7 (10) : 2132 - 2140
  • [9] Green Synthesis of 5-Hydroxymethylfurfural in a Biphasic System Assisted by Microwaves
    Castro, Gabriel Abranches Dias
    Fernandes, Sergio Antonio
    [J]. CATALYSIS LETTERS, 2023, 153 (04) : 984 - 994
  • [10] Clayden J., 2001, ORGANIC CHEM