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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266011Generated: October 27, 2026

Water → 7beta-Ethyl-estra-1,3,5(10)-trien-17-one

https://huagongshe.com/reaction/1266011

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) δ0.91 (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 numberUS06548491B2
Source datasetuspto-grants-2003_04
ORD IDord-5971124618e948f8aa8ab07d6c6cbf50
Source noteuspto-grants-2003_04