HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1005310Generated: October 27, 2026
Water → 7beta-Ethyl-estra-1,3,5(10)-trien-17-one
https://huagongshe.com/reaction/1005310
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 7beta-Ethyl-estr-4-ene-3,17-dione | HCID 15455041 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7beta-Ethyl-estra-1,3,5(10)-trien-17-one | HCID 57179861 | 84.7% |
Reaction Steps
To a solution of enone 55 (0.35 g, 1.17 mmol) in acetonitrile (10 mL) was added a CuBr2 (0.31 g, 1.4 mmol) and stirred overnight at room temperature. Water was added until disappearance of the green color, and the acetonitrile was removed under reduced pressure. The residue was extracted with EtOAc. The combined organic layers were dried over anhydrous MgSO4, filtered, and the combined organic layers were washed with water; brine, dried over anhydrous MgSO4, filtered, and concentrated to afford a gum. Chromatography (20% EtOAc/hexane) yielded estrone 56 as a yellow solid (0.28 g, 80%): The major 7α-ethyl isomer of 56: 1H NMR (300 MHz, CDCl3) δ 0.91 (s, 3, CH3), 0.95 (t, J=7.3 Hz, 3, CH2CH3), 6.59 (d, J=2.5 Hz, 1, ArH), 6.65 (dd, J=2.5, 8.4 Hz, 1, ArH), 7.13 (d, J=8.4 Hz, 1, ArH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06054446 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-344823776e314b7dbd7536bca535941e |
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| Source note | uspto-grants-2000_04 |
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