Extraction method of 2-(2-phenethyl) chromone components in agalloch eaglewood and application of 2-(2-phenethyl) chromone components
A kind of technology of Qinan agarwood and extraction method, which is applied in the field of extraction of 2-chromone components in Qinan agarwood, and can solve the problems of side effects, insignificant effect, easy recurrence and the like.
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Embodiment 1
[0034] The rapid preparation of two 2-(2-phenylethyl) chromones of embodiment 1
[0035] Take 100g of dried Agarwood chinensis, put it into a flash extractor after crushing, add 5 times of 75% ethanol, stir at a high speed (6000 times / min) at room temperature to break the cell tissue wall, extract for 1min, and then After putting it into a cold storage at 4° C. for 12 hours, filter to obtain the supernatant. Concentrate by flash evaporation at 45°C to obtain agarwood extract. The agarwood extract was separated at a vacuum degree of 300mTorr, a heating temperature of 80°C, a sample injection speed of 3s / drop, and a cooling temperature of 10°C, and the heavy components were collected. The heavy component mixture was separated by Sephadex LH-20 column chromatography, methanol-water (volume ratio 7:3), eluted at a flow rate of 1.5mL / min to obtain 8.4 grams of 2-(2-phenylethyl)chromone, 2 10.2 grams of [2-(4-methoxy)phenethyl]chromone, with a purity of over 93%.
Embodiment 2
[0036] The rapid preparation of two 2-(2-phenylethyl) chromones of embodiment 2
[0037] Take 100g of dried Agarwood chinensis, put it into a flash extractor after crushing, add 8 times of 85% ethanol, stir at a high speed (7500 times / min) at room temperature to break the cell tissue wall, extract for 2min, and then After putting it into a cold storage at 2° C. for 12 h, filter to obtain the supernatant. Concentrate by flash evaporation at 50°C to obtain agarwood extract. The agarwood extract was separated at a vacuum degree of 200mTorr, a heating temperature of 70°C, a sample injection speed of 2s / drop, and a cooling temperature of 8°C, and the heavy components were collected. The heavy component mixture was separated by Sephadex LH-20 column chromatography, methanol-water (volume ratio 8:2), eluted at a flow rate of 1.5mL / min to obtain 9.8 grams of 2-(2-phenylethyl)chromone, 2 11.9 grams of [2-(4-methoxy)phenethyl]chromone, with a purity of over 95%.
Embodiment 3
[0038] The rapid preparation of two 2-(2-phenylethyl) chromones of embodiment 3
[0039]Take 100g of dried Agarwood chinensis, put it into a flash extractor after crushing, add 10 times of 95% ethanol, stir at a high speed (9000 times / min) at room temperature to break the cell tissue wall, extract for 3 minutes, and then After putting it into a cold storage at 0° C. for 12 h, filter to obtain the supernatant. Concentrate by flash evaporation at 55°C to obtain agarwood extract. The agarwood extract was separated at a vacuum degree of 100mTorr, a heating temperature of 60°C, an injection speed of 1s / drop, and a cooling temperature of 5°C, and the heavy components were collected. The heavy component mixture was separated by Sephadex LH-20 column chromatography, methanol-water (volume ratio 10:1), eluted at a flow rate of 1.5mL / min to obtain 11.2 grams of 2-(2-phenylethyl)chromone, 2 13.6 grams of [2-(4-methoxy)phenethyl]chromone, with a purity of over 98%.
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