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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651371Generated: October 25, 2026

Ammonium Chloride → 7beta-Ethyl-estr-4-ene-3,17-dione

https://huagongshe.com/reaction/651371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEstra-4,6-diene-3,17-dioneHCID 128845—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 178461630HCID 178461630—
SolventTetrahydrofuranHCID 8028—
Product7beta-Ethyl-estr-4-ene-3,17-dioneHCID 1545504139%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a mixture of CuI(Bu3P)4 (15.7 g, 40 mmol) in THF (50 mL) was added a 1.0 M solution of EtMgBr in THF (40 mL, 40 mmol) at −30° C., and stirred for 20 min. The reaction mixture was cooled to −78° C. and dione 54 (3.5 g, 12.94 mmol) was added. The reaction mixture was warmed to −30° C. for 0.5 h, and poured into saturated aqueous NH4Cl. The mixture was extracted with EtOAc. The combined organic layers were dried over anhydrous MgSO4, filtered, and then concentrated to afford a solid. Chromatography (20% EtOAc/hexane) yielded dione 55 as a yellow solid (1.5 g, 39%). The major 7α-ethyl isomer of 55: 1H NMR (300 MHz, CDCl3) δ0.89 (T, J=7.0 Hz, 3, CH2CH3), 0.93 (s, 3, CH3), 2.60 (dd, J=2.4, 14.3 Hz, 1), 5.85 (s, 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06281205B1
Source datasetuspto-grants-2001_08
ORD IDord-a6e44ef7dedb42489e2a76e70c92bbc3
Source noteuspto-grants-2001_08