Method for preparing isofraxidin from acanthopanax senticosus rhizomes
A technology of isoqine and Acanthopanax senticosus, which is applied in the field of preparation of isoqine, can solve the problems of complicated operation, low yield and the like, and achieves the effects of simple process, high yield and strong practicability.
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Embodiment 1
[0013] After crushing 500 g of dried and pulverized Acanthopanax roots, use 3000 ml of 50% ethanol solution to extract under reflux at 80° C. for 3 hours, filter the mixture, concentrate the filtrate under reduced pressure to 1 / 2 volume, add 0.6 mol / l aqueous hydrochloric acid, The dosage is 0.5 times the volume of the concentrated solution, the dosage of 1,1-dichloroethane is 2 times the volume of the concentrated solution, the hydrolysis extraction temperature is 85° C., and the time is 5 hours. The 1,1-dichloroethane phase was separated, concentrated to dryness under reduced pressure, and the crude product of isoferidin was obtained, and the extraction rate was 1.25 times that of conventional acid hydrolysis.
Embodiment 2
[0015] After crushing 500 g of dried and pulverized Acanthopanax roots, use 3500 ml of 60% ethanol solution to extract under reflux at 80° C. for 3 hours, filter the mixture, concentrate the filtrate under reduced pressure to 1 / 2 volume, add 0.6 mol / l aqueous hydrochloric acid, The dosage is 0.8 times the volume of the concentrated solution, the dosage of 1,1-dichloroethane is 1.5 times the volume of the concentrated solution, the hydrolysis extraction temperature is 85° C., and the time is 4 hours. The 1,1-dichloroethane phase was separated, concentrated to dryness under reduced pressure, and the crude product of isoferidin was obtained, and the extraction rate was 1.23 times that of traditional acid hydrolysis.
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