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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837244Generated: November 2, 2026

Sodium borohydride → 7alpha-(6-Chlorohexyl)-11beta-fluor-estra-1,3,5(10)-triene-3,17-diol

https://huagongshe.com/reaction/1837244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant7alpha-(6-Chlorohexyl)-11beta-fluor-3-hydroxy-estra-1,3,5(10)-trien-17-oneHCID 15870670—
SolventMethanolHCID 887—
Product7alpha-(6-Chlorohexyl)-11beta-fluor-estra-1,3,5(10)-triene-3,17-diolHCID 6991639797.6%

Reaction Steps

611 mg of 7α-(6-chlorohexyl)-11β-fluor-3-hydroxy-estra-1,3,5(10)-trien-17-one is dissolved in 10 ml of methanol and carefully mixed with 166 mg of sodium borohydride. After 15 minutes of stirring at room temperature, the batch is added to saturated common salt solution, extracted with methylene chloride, dried on magnesium sulfate and concentrated by evaporation in a vacuum. 599 mg of 7α-(6-chlorohexyl)-11β-fluor-estra-1,3,5(10)-triene-3,17-diol is obtained as a crude product, which is used without further purification in the next stage.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06780855B2
Source datasetuspto-grants-2004_08
ORD IDord-2e6239b428c2456d87a99d49f57b7d3e
Source noteuspto-grants-2004_08