Method for preparing dihydroartemisinin bulk drug in single process
A method for preparing dihydroartemisinin bulk drug in single process comprises: S1. dissolving artemisinin in aprotic solvent; S2. adding phase transfer catalyst and reducing agent in sequence to cause a reduction reaction with artemisinin; S3. adjusting the pH of the reaction system obtained in step S2 to 5-7 with acid solution, adding water and stirring, separating the liquids, extracting the aqueous phase obtained by the separation with the same aprotic solvent as in step S1, combining the organic phase obtained by extraction and separation, washing with water, and drying, obtaining dried organic phase; S4. placing the dried organic phase obtained in step S3 in a crystallization device that has the functions of crystallization-press filtration-drying, and then the crystals are precipitated, concentrated, press-filtered, and dried to obtain the refined dihydroartemisinin.
1. A method for preparing dihydroartemisinin bulk drug in a single process, comprising:
S1, dissolving artemisinin in an aprotic solvent;
S2, adding a phase transfer catalyst and a reducing agent in sequence to cause a reduction reaction with the artemisinin;
S3, adjusting a pH of the reaction system obtained in step S2 to 5-7 with an acid solution, adding water and stirring, separating the liquids, extracting an aqueous phase obtained by the separation with the same aprotic solvent as in step S1, combining the organic phases obtained by extraction and separation, washing with water, and drying, obtaining dried organic phase;
S4, placing the dried organic phase obtained in step S3 in a crystallization device that has the functions of crystallization-press filtration-drying, and precipitating crystals, followed by concentrating, press-filtering, and drying the crystals to obtain a refined dihydroartemisinin.
2. The method for preparing dihydroartemisinin bulk drug in a single process according to claim 1 , wherein the aprotic solvent is toluene, methylene chloride, dichloroethane or trichloromethane.
3. The method for preparing dihydroartemisinin bulk drug in a single process according to claim 1 , wherein in step S4, a pressure of the press-filtering is 4-6 kg, and a time of the press-filtering is 20-50 min.
4. The method for preparing dihydroartemisinin bulk drug in a single process according to claim 1 , wherein in step S3, when adjusting the pH of the reaction system with the acid solution, a temperature is controlled to 0-25° C.
5. The method for preparing dihydroartemisinin bulk drug in a single process according to claim 1 , wherein in step S3, the acid solution is acetic acid solution or hydrochloric acid solution, and a mass concentration of the acid solution is 20%-30%.
6. The method for preparing dihydroartemisinin bulk drug in a single process according to claim 5 , wherein in step S3, the acid solution is a 25% mass concentration of an acetic acid solution.
7. The method for preparing dihydroartemisinin bulk drug in a single process according to claim 1 , wherein the phase transfer catalyst is benzyltriethylammonium chloride or tetrabutylammonium bromide.
8. The method for preparing dihydroartemisinin bulk drug in a single process according to claim 1 , wherein an amount of the phase transfer catalyst is 0.3%-0.8% by weight of the artemisinin.
9. The method for preparing dihydroartemisinin bulk drug in a single process according to claim 1 , wherein in step S1, a mass-volume ratio of the artemisinin to the aprotic solvent is 1:4-8 g/mL.
10. The method for preparing dihydroartemisinin bulk drug in a single process according to claim 1 , wherein in step S2, the reducing agent is sodium borohydride or potassium borohydride, and an amount of the reducing agent is 10%-20% by weight of the artemisinin.