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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837033Generated: October 31, 2026

Ethanol → HCID 69790149, compound

https://huagongshe.com/reaction/1837033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantHCID 69789601HCID 69789601—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69790149HCID 6979014997.4%

Reaction Steps

—Sodium borohydride (1.47 g) was added to a solution of (7α)-7-ethenyl-3-methoxyestra-1,3,5(10),14-tetraen-17-one (1.50 g) obtained in the previous step in a mixture of tetrahydrofuran (27.8 ml), ethanol (27.8 ml) and water (4.55 ml). The reaction mixture was stirred for 50 min. and then poured into water. The product was extracted into ethyl acetate. The combined organic phases were washed with water and brine, dried over sodium sulfate and concentrated, to afford (7α,17β)-7-ethenyl-3-methoxyestra-1,3,5(10),14-tetraen-17-ol (1.47 g). The product was used in the following step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780854B2
Source datasetuspto-grants-2004_08
ORD IDord-3e5c98f0bbe6441ab1065cae39df895c
Source noteuspto-grants-2004_08