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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582816Generated: October 25, 2026

Boron trifluoride etherate → 3-Methoxy-7alpha-(2-propenyl)estra-1,3,5(10)-trien-17beta-ol

https://huagongshe.com/reaction/1582816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantPotassium CarbonateHCID 11430—
ReactantTriethylsilaneHCID 12052—
Reactant17beta-Hydroxy-3-methoxy-7alpha-(2-propenyl)estra-1,3,5(10)-trien-6-oneHCID 69415006—
SolventDichloromethaneHCID 6344—
Product3-Methoxy-7alpha-(2-propenyl)estra-1,3,5(10)-trien-17beta-olHCID 6941480798.8%

Reaction Steps

Triethylsilane (5 ml) and boron trifluoride diethyl etherate (5 ml) were added to a solution of 17β-hydroxy-3-methoxy-7α-(2-propenyl)estra-1,3,5(10)-trien-6-one (1.0 g, 2.9 mmol) in dichloromethane (20 mL) at 0° C. The resulting mixture was warmed to room temperature and stirred for 18 hours. After the reaction was completed, 10% aqueous potassium carbonate was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and then filtered. After concentration under reduced pressure, the resulting residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=2/1) to give 3-methoxy-7α-(2-propenyl)estra-1,3,5(10)-trien-17β-ol (935 mg, Yield 98%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737417B2
Source datasetuspto-grants-2004_05
ORD IDord-ff0ccbc9e7024b25818fe3011591c61b
Source noteuspto-grants-2004_05