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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650348Generated: October 28, 2026

Lithium Bromide → 7alpha-(5-Acetoxypentyl)-11beta-fluoro-3-hydroxy-estra-1,3,5(10)-trien-17-one

https://huagongshe.com/reaction/650348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium BromideHCID 82050—
ReactantSodium BicarbonateHCID 516892—
Reactant7alpha-(5-Acetoxypentyl)-11beta-fluorooestr-4-ene-3,17-dioneHCID 69935327—
CatalystCopper bromide (CuBr2)HCID 24611—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product7alpha-(5-Acetoxypentyl)-11beta-fluoro-3-hydroxy-estra-1,3,5(10)-trien-17-oneHCID 6993511951.8%

Reaction Steps

18.6 of copper(II) bromide and 3.6 g of lithium bromide are added to 16.5 g of 7α-(5-acetoxypentyl)-11β-fluoro-estr-4-ene-3,17-dione in 190 ml of acetonitrile at 80° C. After 15 minutes, the reaction mixture is stirred into sodium bicarbonate-containing ice water. The precipitated product is suctioned off, dissolved in ethyl acetate, washed with water, dried and concentrated by evaporation in a vacuum. After the crude product is chromatographed on silica gel with a hexane-ethyl acetate gradient, 8.5 g of 7α-(5-acetoxypentyl)-11β-fluoro-3-hydroxy-estra-1,3,5(10)-trien-17-one is obtained as foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271403B1
Source datasetuspto-grants-2001_08
ORD IDord-ba74732a6bca414eb3cdeed3be18a116
Source noteuspto-grants-2001_08