The method utilizing chitin biomass to produce 5-hydroxymethylfurfural
A technology of hydroxymethylfurfural and chitin, applied in the direction of organic chemistry, etc., to achieve the effect of simple operation process, wide sources and abundant reserves
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Embodiment 1
[0019] (1) Prepare 60 g of zinc chloride aqueous solution with a mass concentration of 30%, add 5 g of chitin with a molecular weight of 400,000, and add 0.5 g of CrCl 3 ·6H 2 O mixed and reacted at 120 °C for 8 hours.
[0020] (2) After the reaction, 75 mL of methyl isobutyl ketone was added as an extractant to extract 5-hydroxymethylfurfural.
[0021] (3) The obtained methyl isobutyl ketone phase in which the product 5-hydroxymethylfurfural is dissolved is concentrated and evaporated to dryness, and the solid obtained after concentration is crystallized in petroleum ether to obtain the 5-hydroxymethylfurfural product, 5-hydroxymethylfurfural The molar yield of furfural is 30%.
Embodiment 2
[0023] (1) Prepare 85 g of zinc chloride aqueous solution with a mass concentration of 67%, add 10 g of chitosan with a molecular weight of 0.1 million and a degree of deacetylation of 100%, and add 10 g of B(OH) 3 , reacted at 100 °C for 5 hours.
[0024] (2) After the reaction, 120 mL of butanol was added as an extractant to extract 5-hydroxymethylfurfural.
[0025] (3) Concentrate and evaporate to dryness the obtained butanol phase in which the product 5-hydroxymethylfurfural is dissolved, and crystallize the obtained solid with benzene to obtain the 5-hydroxymethylfurfural product. The molar yield of the 5-hydroxymethylfurfural product is was 43%.
Embodiment 3
[0027] (1) Prepare 30 g of zinc chloride aqueous solution with a mass concentration of 60%, add 10 g of chitosan with a molecular weight of 120,000 and a degree of deacetylation of 64%, and add 0.2 g of SnCl 4 ·5H 2 O was used as a catalyst for continuous reaction at 135 °C for 10 hours.
[0028] (2) After the reaction, 100 mL of 2,5-dimethylpentanone was added as the extractant to extract the product 5-hydroxymethylfurfural.
[0029] (3) Concentrate and evaporate the obtained 2,5-dimethylpentanone phase to dryness, and crystallize with a mixed solvent of 1,4-dioxane-petroleum ether to obtain 5-hydroxymethylfurfural product, 5-hydroxymethylfurfural The molar yield of furfural product is 35%.
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