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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361682Generated: October 29, 2026

Hydrochloric Acid → 7alpha-(6-Chlorohexyl)-11beta-fluor-3-hydroxy-estra-1,3,5(10)-trien-17-one

https://huagongshe.com/reaction/361682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium BromideHCID 82050—
ReactantSodium BicarbonateHCID 516892—
Reactant7alpha-(6-Chlorohexyl)-11beta-fluoro-estr-4-ene-3,17-dioneHCID 69917938—
CatalystCopper bromide (CuBr2)HCID 24611—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product7alpha-(6-Chlorohexyl)-11beta-fluor-3-hydroxy-estra-1,3,5(10)-trien-17-oneHCID 1587067022.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

28.1 g of copper(II) bromide and 5.4 g of lithium bromide in 105 ml of anhydrous acetonitrile are added to 25.2 g of 7α-(6-chlorohexyl)-11β-fluoro-estr-4-ene-3,17-dione in 175 ml of anhydrous acetonitrile at 80° C. After 15 minutes, the reaction mixture is cooled to 0° C., and 250 ml of saturated sodium bicarbonate solution is added in drops. Then, the solution is stirred into 1 liter of water, brought to pH=6 with 2N hydrochloric acid, extracted 3 times with ethyl acetate, washed with common salt solution, dried on magnesium sulfate and concentrated by evaporation in a vacuum. Chromatography of the crude product on silica gel with a hexane-ethyl acetate gradient yields 5.7g of 7α-(6-chlorohexyl)-11β-fluoro-3-hydroxy-estra-1,3,5(10)-trien-17-one as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866560
Source datasetuspto-grants-1999_02
ORD IDord-50ef4b395a0e41c98b5d2971079a0e6a
Source noteuspto-grants-1999_02