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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 222868Erstellt: 26. Oktober 2026

Diazomethane → (11R)-dihydroartemisinic aldehyde

https://huagongshe.com/reaction/222868

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiazomethaneHCID 9550—
EduktDihydroartemisinic acidHCID 11020893—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(11R)-dihydroartemisinic aldehydeHCID 1085703148%

Reaktionsschritte

Dihydroartemisinic aldehyde was synthesized from the isolated dihydroartemisinic acid. The acid was converted to methyl dihydroartemisinate with excess diazomethane in diethyl ether at 0° C. for 5 minutes. The ether and diazomethane were removed under a stream of nitrogen and the methyl ester was reduced to (11R)-dihydroartemisinic alcohol with excess 1.5 M diisobutyl aluminum hydride in toluene at room temperature for 10 min under nitrogen. With subsequent extraction, oxidation to the aldehyde with pyridinium chlorochromate (Corey & Suggs 1975) and purification by HPLC the (11R)-dihydroartemisinic aldehyde was produced at an overall yield of 48% with >99% purity according to GC analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08207402B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-64d0546a608c489d91651c8366f8319e
Quellennotizuspto-grants-2012_06