Novel phytosterol or/and phytostanol derivative preparation method
A technology for phytosterols and phytosterols, which is applied in the field of preparation of novel phytosterols or/and phytostanol derivatives, can solve the problem that the research on the modification of phytosterols or/and phytosterols is not comprehensive enough and the scope of application is small. And other problems, to achieve the effect of low reaction conditions, improve conversion rate, and broaden the scope of application
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Embodiment 1
[0050] Weigh 12.4g of β-sitosterol, 7.9g of glutaric acid, and 0.4mL of catalyst pyridine into a reflux reaction device pre-added with 200mL of benzene and equipped with stirring and oil bath temperature control. The reaction temperature is controlled at 80°C, every 2 hours Sampling was carried out to detect the reaction progress. After 14 hours of reaction, the sample was taken out by rotary evaporation to remove the solvent to obtain the intermediate product β-sitosterol glutaric acid monoester.
Embodiment 2
[0052] Weigh 1.0 g of β-sitosterol glutaric acid monoester and 0.7 g of glucose in a 50 mL reaction bottle, add 10% of the total mass of β-sitosterol glutaric acid monoester and glucose to the immobilized lipase derived from thermophilic fungi , add 25mL acetone as a solvent, 1.0g molecular sieves, airtight, place in a water bath shaker, control the rotation speed 150rpm, the reaction temperature is 45°C, take samples every 12 hours to detect the reaction process, and react for 72 hours; after high performance liquid chromatography analysis, the reaction solution The purity of β-sitosterol glucoglutarate in the medium is 65%; the water-soluble β-sitosterol derivative-sitosterol glucoglutarate with a purity of more than 95% is obtained through separation and purification by column chromatography.
Embodiment 3
[0054] Weigh 12.5g of sitostanol, 10.4g of suberic acid, and 0.5g of copper dodecyl sulfate as a catalyst, and add it to a reflux reaction device with 200mL of toluene added in advance and equipped with stirring and oil bath temperature control, and the reaction temperature is controlled at 110°C , Sampling every 2 hours to detect the reaction process, reacting for 12 hours, taking out the sample and rotary evaporating to remove the solvent to obtain the intermediate product sitostanol suberic acid monoester.
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