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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084724Generated: October 30, 2026

Iodine → HCID 131724403, compound

https://huagongshe.com/reaction/2084724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantOxygenHCID 977—
ReactantIsopropanolHCID 3776—
ReactantSodium ThiosulfateHCID 24477—
Reactant(+)-Estr-4-ene-3,17-dioneHCID 92834—
SolventAcetonitrileHCID 6342—
ProductHCID 131724403HCID 13172440340%

Reaction Steps

Iodine (7.61 g, 30 mmol) and 19-nor-4-androstene-3,17-dione (2.72 g, 10 mmol) were dissolved in a mixture of acetonitrile (75 mL) and isopropanol (75 mL), to thereby form a reaction mixture. The reaction mixture was stirred for two hours while oxygen was introduced (50 mL/min) thereto under cooling in an ice-bath. The resultant mixture was maintained at room temperature, and after stirring of the mixture for a further 1.5 hours, introduction of oxygen was stopped and the mixture was refluxed for one hour. The reaction mixture was cooled to room temperature, and an aqueous solution of sodium thiosulfate was added to the mixture. The mixture was extracted with chloroform, and the organic phase was washed sequentially with an aqueous solution of sodium bicarbonate and saturated brine. The washed matter was dried over magnesium sulfate anhydrate, filtered, and evaporated under reduced pressure. The formed precipitates were recrystallized from acetone, to thereby yield 1.3 g of the title compound (yield 40%). The remaining mother liquor was purified through silica gel column chromatography (chloroform), to thereby further obtain 1.3 g of the title compound (overall yield: 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06717002B2
Source datasetuspto-grants-2004_04
ORD IDord-70b193bfed484a069ee008ad5a66e5b4
Source noteuspto-grants-2004_04