Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196329Generated: November 1, 2026

p-Toluenesulfonic acid → 3-Oxopregna-1,4,6-triene-20-carbaldehyde

https://huagongshe.com/reaction/1196329

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant20-(5,5-Dimethyl-1,3-dioxan-2-yl)pregna-1,4,6-trien-3-oneHCID 22843932—
SolventAcetoneHCID 180—
Product3-Oxopregna-1,4,6-triene-20-carbaldehydeHCID 2284388575%

Reaction Steps

In 100 ml of acetone was dissolved 0.410 g (1.0 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)pregna-1,4,6-trien-3-one, followed by addition of 10 mg (0.05 mmole) of p-toluenesulfonic acid. The mixture was stirred at room temperature for 12 hours. From the reaction mixture thus obtained, the solvent was distilled off under reduced pressure and the residue was diluted with methylene chloride. The methylene chloride solution was washed successively with saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium chloride solution and dried over magnesium sulfate. The solvent was then distilled off under reduced pressure and the residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane=1:5, v/v) to recover 0.243 g of 3-oxopregna-1,4,6-triene-20-carbaldehyde (yield: 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112998
Source datasetuspto-grants-1992_05
ORD IDord-ccdd53005fa744c4b8547bbbda92811a
Source noteuspto-grants-1992_05