[go: up one dir, main page]

Wagh et al., 2020 - Google Patents

An efficient heterogeneous acid catalyst DICAT-1 for one-pot conversion of sucrose into 5-(hydroxymethyl) furfural

Wagh et al., 2020

Document ID
16688800170152781833
Author
Wagh A
Pawar H
Publication year
Publication venue
Energy & Fuels

External Links

Snippet

5-(Hydroxymethyl) furfural (HMF) is a trending biogenic platform molecule for the production of multiple energy, fuel, and chemical products, and it can be synthesized by using C6 sugars and/or its oligomers and polymers. In the present paper, the heterogeneous solid …
Continue reading at pubs.acs.org (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/40Radicals substituted by oxygen atoms
    • C07D307/46Doubly bound oxygen atoms, or two oxygen atoms singly bound to the same carbon atom
    • C07D307/48Furfural
    • C07D307/50Preparation from natural products
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/40Radicals substituted by oxygen atoms
    • C07D307/42Singly bound oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/58One oxygen atom, e.g. butenolide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/56Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/68Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/10Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms

Similar Documents

Publication Publication Date Title
Aranha et al. A review on green and efficient synthesis of 5-hydroxymethylfurfural (HMF) and 2, 5-furandicarboxylic acid (FDCA) from sustainable biomass
Zhang et al. Catalytic transformation of lignocellulose into chemicals and fuel products in ionic liquids
Tiong et al. Conversion of biomass and its derivatives to levulinic acid and levulinate esters via ionic liquids
Xiao et al. Efficient conversion of cellulose into biofuel precursor 5-hydroxymethylfurfural in dimethyl sulfoxide–ionic liquid mixtures
Choudhary et al. Conversion of xylose to furfural using Lewis and Brønsted acid catalysts in aqueous media
Hu et al. Efficient conversion of glucose into 5-hydroxymethylfurfural by chromium (III) chloride in inexpensive ionic liquid
Zakrzewska et al. Ionic liquid-mediated formation of 5-hydroxymethylfurfural A promising biomass-derived building block
Zhao et al. Continuous flow alcoholysis of furfuryl alcohol to alkyl levulinates using zeolites
Ngee et al. Sulfated mesoporous niobium oxide catalyzed 5-hydroxymethylfurfural formation from sugars
Garcés et al. Aqueous phase conversion of hexoses into 5-hydroxymethylfurfural and levulinic acid in the presence of hydrochloric acid: mechanism and kinetics
Tucker et al. Sustainable solvent systems for use in tandem carbohydrate dehydration hydrogenation
Pagan-Torres et al. Production of 5-hydroxymethylfurfural from glucose using a combination of Lewis and Brønsted acid catalysts in water in a biphasic reactor with an alkylphenol solvent
Hu et al. Acid-catalyzed conversion of xylose in 20 solvents: insight into interactions of the solvents with xylose, furfural, and the acid catalyst
Román-Leshkov et al. Activation of carbonyl-containing molecules with solid Lewis acids in aqueous media
Ding et al. Catalytic conversion of cellulose to 5-hydroxymethyl furfural using acidic ionic liquids and co-catalyst
Daengprasert et al. Application of sulfonated carbon-based catalyst for solvothermal conversion of cassava waste to hydroxymethylfurfural and furfural
Li et al. Kinetics of furfural production from corn cob in γ-valerolactone using dilute sulfuric acid as catalyst
Rathod et al. Metal free acid base catalyst in the selective synthesis of 2, 5-diformylfuran from hydroxymethylfurfural, fructose, and glucose
Li et al. Catalytic alkylation of 2-methylfuran with formalin using supported acidic ionic liquids
Zhang et al. Catalyzing Cascade Production of Methyl Levulinate from Polysaccharides Using Heteropolyacids H n PW11MO39 with Brønsted/Lewis Acidic Sites
Tang et al. Dehydration of carbohydrates to 5-hydroxymethylfurfural over lignosulfonate-based acidic resin
Boonyakarn et al. Enhanced levulinic acid production from cellulose by combined Brønsted hydrothermal carbon and Lewis acid catalysts
Wagh et al. An efficient heterogeneous acid catalyst DICAT-1 for one-pot conversion of sucrose into 5-(hydroxymethyl) furfural
Naim et al. Toward an Intensified Process of Biomass-Derived Monomers: the Influence of 5-(Hydroxymethyl) furfural byproducts on the gold-catalyzed synthesis of 2, 5-furandicarboxylic acid
Huang et al. Clean synthesis of 5-hydroxymethylfurfural and levulinic acid by aqueous phase conversion of levoglucosenone over solid acid catalysts