A kind of method for extracting tripterygium chloractone from tripterygium wilfordii extract
A technology for tripterygium chloractone and tripterygium, which is applied in the field of extracting single-component tripterygium chloractone, can solve the problems of small amount of tripterygium chloractone, low extraction yield, and inability to be used in large-scale production. Achieve the effects of increasing the content of tripterygium chloractone, simplifying the separation and purification process, and making the purification process simple and easy
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Embodiment 1
[0016] Take 4100g of the concentrated extract of the front part of Tripterygium wilfordii, add 4500ml of acetone and 400ml of hydrochloric acid, put it in a 10000ml round bottom flask, put it in a water bath and heat it to reflux at 80°C, and react for 2 hours when it starts to reflux, take it out, add 4500ml of purified water, and use plastic Stir the rod evenly and let it stand overnight; the next day separate the upper acetone solution, filter it with filter paper, put the filtrate on a water bath at 65°C to recover acetone (600ml per 2000ml), then adjust it to 80°C to recover about 1000ml of concentrated solution, pour The filtrate was extracted three times with chloroform, and the extract was dried under reduced pressure after recovering the chloroform to obtain 241.986 g of the transformed product powder. The conversion product was applied to a silica gel column at a ratio of 1:10, ethanol-chloroform gradient elution, T4 was collected, drained, and the dried product was r...
Embodiment 2
[0018] Take 30Kg of the concentrated extract of Tripterygium wilfordii, add ethanol 90Kg, hydrochloric acid 1800ml, heat and reflux with steam in the enamel reaction pot for 6 hours, put it in a plastic storage bucket, add 90Kg of water, turn on the mixer and stir for 15 minutes, and let it stand overnight; the next day vacuum Aspirate the upper layer solution, recover ethanol in the enamel reaction pot, release it when it is concentrated to about 1 / 3, add chloroform to the filtrate and extract three times, the extract is dried under reduced pressure after recovering chloroform to obtain 7.215Kg of crude extract powder (yield 24.05% ). Put the crude extract powder into a large stainless steel column (30×500cm) for silica gel chromatography to obtain 1343.3 g of fine extract powder. The fine extract powder was recrystallized twice with chloroform to obtain 161.2 g of white crystals with a measured content of 98.5% triptolide.
Embodiment 3
[0020] Take 100Kg of the concentrated extract of the front part of Tripterygium wilfordii, add methanol 500Kg, hydrochloric acid 20L, steam heat and reflux in the enamel reaction pot for 6 hours, put it in a plastic storage bucket, add 500Kg of water, turn on the mixer and stir for 15 minutes, and let it stand overnight; the next day vacuum Aspirate the upper layer solution, recover methanol in the enamel reaction pot, release it when concentrated to about 1 / 3 of the volume, add chloroform to the filtrate and extract three times, the extract is dried under reduced pressure after recovering chloroform to obtain 20.14Kg of crude extract powder (yield 20.14% ). Put the crude extract powder into a large stainless steel column (30×500cm) for silica gel chromatography to obtain 2348.6 g of fine extract powder. The fine extract powder was recrystallized twice with chloroform to obtain 422.75 g of white crystals with a measured content of 99.01% triptolide.
[0021] The high-performa...
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