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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708762Generated: October 31, 2026

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

https://huagongshe.com/reaction/1708762

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 numberUS05359055
Source datasetuspto-grants-1994_10
ORD IDord-4987a94af035478fa2b499315b055c94
Source noteuspto-grants-1994_10