Conversion of carbohydrates to hydroxymethylfurfural (hmf) and derivatives
OwnerAlexandra J. SANBORN, Stephen J. Howardinventors
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OwnerAlexandra J. SANBORN, Stephen J. Howardinventors
Estimating the term…
A method of producing substantially pure HMF, HMF esters and other derivatives from a carbohydrate source by contacting the carbohydrate source with a solid phase catalyst. A carbohydrate starting material is heated in a solvent in a column and continuously flowed through a solid phase catalyst in the presence of an organic acid, or heated with the organic acid and a solid catalyst in solution to form a HMF ester. Heating without organic acid forms HMF. The resulting product is purified by filtration to remove the unreacted starting materials and catalyst. The HMF ester or a mixture of HMF and HMF ester may then be oxidized to 2,5-furandicarboxylic acid (FDCA) by combining the HMF ester with an organic acid, cobalt acetate, manganese acetate and sodium bromide under pressure. Alternatively, the HMF ester may be reduced to form a furan or tetrahydrofuran diol.
A method for synthesizing HMF by contacting a carbohydrate source with a solid phase catalyst.
A method of preparing HMF esters comprising:
A method for synthesizing HMF by contacting an HMF ester with an anionic solid phase catalyst.
A method for synthesizing citrate esters by contacting a solution having a citrate source and an alcohol with a solid phase catalyst by eluting the solution through a column packed with the solid phase catalyst to obtain an eluant.
A method for synthesizing a levulinic acid comprising the steps of:
A method for synthesizing a levulinate ester comprising the steps of:
A method for synthesizing HMF by contacting a fructose source with an organic acid and solid phase catalyst in a column to produce HMF ester, and
A method for synthesizing a levulinate ester comprising the steps of:
Dependencies are inferred from the claim text.