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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant7beta-Ethyl-estr-4-ene-3,17-dioneHCID 15455041—
ReactantEthyl acetate hexaneHCID 21226206—
SolventAcetonitrileHCID 6342—
Product7beta-Ethyl-estra-1,3,5(10)-trien-17-oneHCID 5717986184.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06054446
Source datasetuspto-grants-2000_04
ORD IDord-344823776e314b7dbd7536bca535941e
Source noteuspto-grants-2000_04