Method for preparing high-purity ursolic acid from salvia
A ursolic acid, high-purity technology, applied in the field of natural medicine, can solve the problems of small sample loading, unfavorable industrial production, low yield and the like, and achieve the effects of small processing volume, easy processing volume and high yield
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Embodiment 1
[0014] Get 1Kg of dry sage leaves, crush them, pass through a 20-mesh sieve, add 12L of petroleum ether, soak for 24 hours at room temperature, filter out the petroleum ether, dry the leaf powder, soak the dry leaf powder with 2L of acetone at room temperature for 10 hours, and then pour it into Continue to add 8L of acetone to the leaf powder, reflux extraction for 2 hours, repeat 2-3 times, combine the acetone extract, filter, concentrate the extract to 3L, filter while hot, and place the clarified filtrate at 4°C for 24 hours. A large amount of yellow-white precipitate was precipitated, which was crude ursolic acid, which was filtered by suction and dried in vacuum. The crude ursolic acid was weighed to be 97g. Wash the crude ursolic acid with 600ml of chloroform and petroleum ether mixed solution with a volume ratio of 1:2, filter with suction, vacuum-dry the filter cake, weigh 74g, add 500ml of acetone and 5g of activated carbon to the filter cake, and heat at 50-60°C Sti...
Embodiment 2
[0016] Get 1Kg of dry sage leaves, crush them, pass through a 20-mesh sieve, add 12L of petroleum ether, soak for 24 hours at room temperature, filter out the petroleum ether, dry the leaf powder, soak the dry leaf powder with 2L of acetone at room temperature for 10 hours, and then pour it into Continue to add 8L of acetone to the leaf powder, reflux extraction for 2 hours, repeat 2-3 times, combine the acetone extract, filter, concentrate the extract to 1L, filter while hot, and place the clarified filtrate at 4°C for 24 hours. A large amount of yellow precipitate was precipitated, which was the crude product of ursolic acid. It was suction filtered and dried in vacuum. The crude product of ursolic acid was weighed to be 164g. Recrystallize once with 800ml of acetone, filter with suction, dry in vacuo, then dissolve the crude product with 400ml of ethanol-acetic acid mixed solution with a volume ratio of 1:1, add 4g of activated carbon, stir at 50-60°C for 1 hour, filter out ...
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