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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815783Generated: October 30, 2026

Ethanol → HCID 69790149, compound

https://huagongshe.com/reaction/1815783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantHCID 69789601HCID 69789601—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69790149HCID 6979014996.3%

Reaction Steps

—Sodium borohydride (8.54 g) was added to a solution of (7α)-7-ethenyl-3-methoxyestra-1,3,5(10),14-tetraen-17-one (8.72 g) in a mixture of tetrahydrofuran (161 ml), ethanol (161 ml), and water (26.4 ml). The reaction mixture was stirred at room temperature for 50 min. and then poured into water. The product was extracted into ethyl acetate; the combined organic phases were washed with water, a saturated aqueous solution of sodium hydrogencarbonate and brine, dried over sodium sulfate and concentrated under reduced pressure. Column chromatography afforded (7α,17β)-7-ethenyl-3-methoxyestra-1,3,5(10),14-tetraen-17-ol (8.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881728B1
Source datasetuspto-grants-2005_04
ORD IDord-08213aa6d12240d39e7267395f5d1fab
Source noteuspto-grants-2005_04