HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582816Generated: October 25, 2026
Boron trifluoride etherate → 3-Methoxy-7alpha-(2-propenyl)estra-1,3,5(10)-trien-17beta-ol
https://huagongshe.com/reaction/1582816
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 17beta-Hydroxy-3-methoxy-7alpha-(2-propenyl)estra-1,3,5(10)-trien-6-one | HCID 69415006 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methoxy-7alpha-(2-propenyl)estra-1,3,5(10)-trien-17beta-ol | HCID 69414807 | 98.8% |
Reaction Steps
Triethylsilane (5 ml) and boron trifluoride diethyl etherate (5 ml) were added to a solution of 17β-hydroxy-3-methoxy-7α-(2-propenyl)estra-1,3,5(10)-trien-6-one (1.0 g, 2.9 mmol) in dichloromethane (20 mL) at 0° C. The resulting mixture was warmed to room temperature and stirred for 18 hours. After the reaction was completed, 10% aqueous potassium carbonate was added to the reaction mixture, which was then extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and then filtered. After concentration under reduced pressure, the resulting residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=2/1) to give 3-methoxy-7α-(2-propenyl)estra-1,3,5(10)-trien-17β-ol (935 mg, Yield 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06737417B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-ff0ccbc9e7024b25818fe3011591c61b |
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| Source note | uspto-grants-2004_05 |
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