HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837245Generated: November 2, 2026
Sodium Iodide → 11beta-Fluor-7alpha-(6-iodohexyl)-estra-1,3,5(10)-triene-3,17-diol
https://huagongshe.com/reaction/1837245
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 7alpha-(6-Chlorohexyl)-11beta-fluor-estra-1,3,5(10)-triene-3,17-diol | HCID 69916397 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 11beta-Fluor-7alpha-(6-iodohexyl)-estra-1,3,5(10)-triene-3,17-diol | HCID 69917772 | 94.3% |
Reaction Steps
599 mg of 7α-(6-chlorohexyl)-11β-fluor-estra-1,3,5(10)-triene-3,17-diol is dissolved in 10 ml of ethylmethylketone, mixed with 675 mg of sodium iodide and stirred overnight at a bath temperature of 90° C. For working-up, the reaction mixture is cooled to room temperature, taken up in ethyl acetate, extracted once with 10% sodium thiosulfate solution, washed with common salt solution, dried on magnesium sulfate and concentrated by evaporation in a vacuum. 691 mg of 11β-fluor-7α-(6-iodohexyl)-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06780855B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-9d56a7408c55447b9b184db2181effb6 |
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| Source note | uspto-grants-2004_08 |
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