Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427762Generated: October 30, 2026

Ethanol → HCID 69790149, compound

https://huagongshe.com/reaction/427762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 69789601HCID 69789601—
SolventWaterHCID 962—
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 tetrahydrofliran (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 fiLrther purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313108B1
Source datasetuspto-grants-2001_11
ORD IDord-a6af34a87c81431b9b965e873c58fd17
Source noteuspto-grants-2001_11