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HRID 1671718Erstellt: 26. Oktober 2026

Water → (E)-Methyl 3alpha-acetoxy-5beta-chol-9(11),16,22-trien-24-oate

https://huagongshe.com/reaction/1671718

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktMethyl propiolateHCID 13536—
EduktEthyl aluminium dichlorideHCID 16686341—
Edukt(3R,5R,8S,10S,13S,14S,Z)-17-Ethylidene-10,13-dimethyl-2,3,4,5,6,7,8,10,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[A]phenanthren-3-YL acetateHCID 25145012—
LösungsmittelDichloromethaneHCID 6344—
Produkt(E)-Methyl 3alpha-acetoxy-5beta-chol-9(11),16,22-trien-24-oateHCID 2514501168%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

Ethyl aluminum dichloride (104.5 mL, 192 mmol, 1.8 M in toluene) was added to a solution of methyl propiolate (13.58 mL, 153 mmol) in DCM (100 mL) at 0° C. under inert atmosphere. The resulting solution was stirred for 15 min and then compound 1.6a (22 g, 64.3 mmol) was added. After stirring for an additional 20 min at 0° C., the temperature was raised to 25° C. and held there for a further 18 h. At this point the reaction was determined to be complete by TLC, and the mixture was poured into cold (0° C.) water (200 mL). The phases were separated and the aqueous layer was extracted with DCM (150 mL). The organic layers were combined and washed sequentially with water (200 mL) and saturated brine solution (100 mL). It was then dried over anhydrous Na2SO4 (40 g) and filtered. The filtrate was concentrated under vacuum and the resulting solid was purified by slurring in methanol (280 mL) to provide compound 1.7a (17.5 g 68%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07994351B2
Quelldatensatzuspto-grants-2011_08
ORD IDord-53a49144e37b43e98b57ed67f34a2b7d
Quellennotizuspto-grants-2011_08