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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 7alpha-(6-Chlorohexyl)-11beta-fluor-3-hydroxy-estra-1,3,5(10)-trien-17-one | HCID 15870670 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 11beta-Fluoro-3-hydroxy-7alpha-(6-iodo-hexyl)oestra-1,3,5(10)-trien-17-one | HCID 57002511 | 102.8% |
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
| 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-f607eb2099514831b339d4ec85247f17 |
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| Source note | uspto-grants-2004_08 |
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