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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Bromide | HCID 82050 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 7alpha-(6-Chlorohexyl)-11beta-fluoro-estr-4-ene-3,17-dione | HCID 69917938 | — |
| Catalyst | Copper bromide (CuBr2) | HCID 24611 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7alpha-(6-Chlorohexyl)-11beta-fluor-3-hydroxy-estra-1,3,5(10)-trien-17-one | HCID 15870670 | 22.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05866560 |
|---|
| Source dataset | uspto-grants-1999_02 |
|---|
| ORD ID | ord-50ef4b395a0e41c98b5d2971079a0e6a |
|---|
| Source note | uspto-grants-1999_02 |
|---|