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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837230Generated: November 3, 2026

Water → 11beta-Fluoro-3-hydroxy-7alpha-(6-iodo-hexyl)oestra-1,3,5(10)-trien-17-one

https://huagongshe.com/reaction/1837230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium IodideHCID 5238—
Reactant7alpha-(6-Chlorohexyl)-11beta-fluor-3-hydroxy-estra-1,3,5(10)-trien-17-oneHCID 15870670—
SolventMethyl Ethyl KetoneHCID 6569—
Product11beta-Fluoro-3-hydroxy-7alpha-(6-iodo-hexyl)oestra-1,3,5(10)-trien-17-oneHCID 57002511102.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

2.7 g of 7α-(6-chlorohexyl)-11β-fluoro-3-hydroxy-estra-1,3,5(10)-trien-17-one is dissolved in 40 ml of ethylmethylketone, mixed with 3.0 g of sodium iodide and stirred overnight at a bath temperature of 90° C. For working-up, the reaction mixture is cooled to room temperature, stirred into water, extracted 3 times with ethyl acetate, washed with common salt solution, dried on magnesium sulfate and concentrated by evaporation in a vacuum. 3.4 g of 11β-fluoro-3-hydroxy-7α-(6-iodohexyl)-estra-1,3,5(10)-trien-17-one 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-f607eb2099514831b339d4ec85247f17
Source noteuspto-grants-2004_08