Method for preparing tetrabenzyl pyran type hexose
A technology of tetrabenzylpyran-type and six-carbon sugar, which is applied in the preparation of sugar derivatives, chemical instruments and methods, sugar derivatives, etc., to achieve the effects of less side reactions, simplified post-treatment methods, and improved purity and yield
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Embodiment 1
[0038] 1) Weigh 0.1 mol of tetrabenzyl glucoside and 0.5 mol of methanol, and stir until completely mixed;
[0039] 2) Add a catalyst to the above reaction system, carry 0.01 mol of sulfuric acid-hydrofluoric acid on silica gel (based on H content), and react at 100°C for 15 hours;
[0040] 3) Filtrate, wash the filter cake with methanol, combine the filtrate and washings, concentrate under reduced pressure at 40°C to a solid, add 0.3mol of ethyl acetate, dissolve, stir and crystallize at 0°C for 5 hours, and obtain 0.086mol of tetrabenzylglucose with a purity of It was 98.3%, and the yield was 86%.
Embodiment 2
[0042] 1) Weigh 0.1 mol of tetrabenzyl glucoside and 0.8 mol of methanol, and stir until completely mixed;
[0043] 2) Add a catalyst to the above reaction system, carry 0.012mol of sulfuric acid-hydrofluoric acid on silica gel (based on H content), and react at 100°C for 18h;
[0044] 3) Filtrate, wash the filter cake with methanol, combine the filtrate and washings, concentrate under reduced pressure at 40°C to a solid, add 0.3mol of ethyl acetate, dissolve, stir and crystallize at 3°C for 5 hours, and obtain 0.088mol of tetrabenzylglucose with a purity of It was 98.1%, and the yield was 88%.
Embodiment 3
[0046] 1) Weigh 0.1 mol of tetrabenzyl glucoside and 1.0 mol of methanol, and stir until completely mixed;
[0047] 2) Add a catalyst to the above reaction system, 0.015mol of sulfuric acid-hydrofluoric acid supported on silica gel (based on H content), and react at 100°C for 20h;
[0048] 3) Filtrate, wash the filter cake with methanol, combine the filtrate and washings, concentrate under reduced pressure at 40°C to a solid, add 0.3mol of ethyl acetate, dissolve, stir and crystallize at 5°C for 5 hours, and obtain 0.087mol of tetrabenzylglucose with a purity of It was 98.3%, and the yield was 87%.
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