Method for preparing alkylglycoside by using solid-carrying heteropolyacid catalyst
A technology for immobilizing heteropolyacids and alkyl glycosides, which is applied in the field of preparation of alkyl glycosides, can solve the problems of poor quality of alkyl glycosides, low glucose conversion rate, easy polymerization, etc., and achieves no environmental pollution, simple operation, selective effect
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Embodiment 1
[0017] Add 100g of anhydrous glucose, 185g of n-butanol and 5g of immobilized phosphotungstic acid (22.5% of immobilized capacity) into a three-necked flask with a stirrer, heat and stir at 100°C, and continue the reaction for 1.5h after the reaction solution is clarified. After the reaction, the catalyst was filtered off. After cooling slightly, 186.3 g of dodecyl alcohol was added to the above reaction system, and heated and stirred at 120° C. for 2 h. After the reaction is finished, cool down, add 2 times the volume of water to the reaction solution for extraction, and then evaporate excess water and n-butanol at 2 mmHg to obtain dodecyl glucoside.
Embodiment 2
[0019] Add 100g of anhydrous glucose, 296.4g of n-butanol and 8g of immobilized silicotungstic acid (14.5% of immobilized capacity) into a three-neck flask with a stirrer, heat and stir at 130°C, and continue the reaction for 2 hours after the reaction solution is clarified. After the reaction, the catalyst was filtered off. After cooling slightly, 198g of decanol was added to the above reaction system, and heated and stirred at 120°C for 3h. Cool after the reaction, add 4 times the volume of the reaction liquid H 2 O-NaCl mixed solution extraction (wherein H 2 (0:NaCl=1:0.05), and then evaporate excess water and n-butanol under 10mmHg to obtain dedecyl glucoside.
Embodiment 3
[0021] Add 100g of anhydrous glucose, 111.2g of n-butanol and 10g of immobilized phosphotungstic acid (34.5% of immobilized capacity) into a three-necked flask with a stirrer, heat and stir at 90°C, and continue the reaction for 3 hours after the reaction solution is clarified. After the reaction, the catalyst was filtered off. After cooling slightly, 195 g of octanol was added to the above reaction system, and heated and stirred at 120° C. for 2 h. Cool after the reaction, add 3 times the volume of the reaction liquid H 2 O-NaCl mixed solution extraction (wherein H 2 O:NaCl=1:0.1), and then evaporate excess water and n-butanol under 4mmHg to obtain octaalkyl glycoside (octyl glycoside).
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