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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748228Generated: November 1, 2026

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

https://huagongshe.com/reaction/1748228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl propiolateHCID 13536—
ReactantEthyl aluminium dichlorideHCID 16686341—
Reactant(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—
SolventDichloromethaneHCID 6344—
Product(E)-Methyl 3alpha-acetoxy-5beta-chol-9(11),16,22-trien-24-oateHCID 2514501168%

Reaction Conditions

Temperature25 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150607B2
Source datasetuspto-grants-2015_10
ORD IDord-c122f1adbf3e40f9bfa2366fa242dba8
Source noteuspto-grants-2015_10