Preparation method of directly extracting and synthesizing chenodeoxycholic acid and ursodeoxycholic acid from pig gall paste or leftovers
A technology of chenodeoxycholic acid and ursodeoxycholic acid, which is applied in the field of preparation of direct extraction and synthesis of chenodeoxycholic acid and ursodeoxycholic acid, can solve the problem of low yield, unsuitable production, and ursodeoxycholic acid Problems such as high cost, to achieve the effect of simplifying the process and reducing the cost
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Embodiment 1
[0034] Get 100 kilograms of pig bile paste, saponify, extract hyodeoxycholic acid (fusing point 175 ℃), after saponification, leftovers contain 30% chenodeoxycholic acid. Direct pretreatment, add 20 times of alkaline water, temperature 95 ° C, ph9 / 10, add 1+1 natural clarifier (Ⅲ-B, produced by Shandong Yaosheng Biotechnology Co., Ltd.) 5 / 10,000 (calculated based on mother liquor). Stir for 4 hours until clarification, cool down, press filter to obtain clarified mother liquor, adjust ph3-4. To obtain pretreated raw materials, add 10 times the amount of methanol, dissolve and cool down to 0°C, add 12.25 kg of bromine solution, stir, for 8 hours, then add sodium carbonate 10% alkaline water to dissolve and wash to remove chenodeoxycholic acid in thin layer chromatography Impurity cholic acid. Apply macroporous weakly basic adsorption resin in ethanol solution to remove bromate and hypobromite to obtain 7-ketolithocholic acid, which contains a small amount of C3 and C7-diketone ...
Embodiment 2
[0036] Referring to Example 1, ursodeoxycholic acid was obtained by reduction with potassium metal.
Embodiment 3
[0038] Referring to Implementation 1, ursodeoxycholic acid was obtained by reduction with Raney nickel.
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