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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1746628Erstellt: 26. Oktober 2026

Oxygen → Qing Hau Sau

https://huagongshe.com/reaction/1746628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxygenHCID 977—
EduktTrifluoroacetic acidHCID 6422—
EduktDihydroartemisinic acidHCID 11020893—
Katalysator5,10,15,20-Tetraphenyl-21,22-dihydroporphyrinHCID 70186—
LösungsmittelDichloromethaneHCID 6344—
ProduktQing Hau SauHCID 983867550%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of dihydroartemisinic acid (4) (1.18 g, 5.0 mmol) and tetraphenylporphyrin (12 mg, 20 μmol) in dichloromethane (total volume of the solution: 10.0 mL, volumetric flask) was prepared. The lamp was turned on 30 min prior to the beginning of the experiment. The reactor was flushed with pure dichloromethane (2.5 mL/min) and oxygen (5 mL/min, 11.5 bar) for 5 min. The reagents were then injected at a flow rate of 2.5 mL/min and the flow of oxygen was readjusted to 5 mL/min (11.5 bar). After the injection of the entire solution of (4), the reactor was flushed with pure dichloromethane (2.5 mL/min) to recover all material. The reaction mixture was collected in a round bottom flask and was cooled down to 0° C. Oxygen was bubbled into the reaction mixture at atmospheric pressure. After 2 min of bubbling, TFA (0.19 mL, 2.5 mmol, 0.5 eq.) was added drop wise. The resulting mixture was stirred at 0° C. for 2 h, while maintaining the oxygen bubbling. Then, the reaction was quenched with a saturated aqueous solution of NaHCO3. The resulting biphasic mixture was stirred at room temperature until disappearance of the green colour. The phases were separated and the aqueous phase was extracted with dichloromethane (3 times). The combined organic layers were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. Purification over silica gel (5%-20% EtOAc in cyclohexane) afforded artemisinin (0.707 g, 50%) as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09150535B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-3149545054a343a380fbd3d4100b75c5
Quellennotizuspto-grants-2015_10