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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196331Generated: October 29, 2026

Acetone → 6alpha,7alpha-Diepoxy-3-oxopregn-4-ene-20-carbaldehyde

https://huagongshe.com/reaction/1196331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactant6alpha,7alpha-Diepoxypregn-4-en-3oneHCID 86745798—
Product6alpha,7alpha-Diepoxy-3-oxopregn-4-ene-20-carbaldehydeHCID 8674580655%

Reaction Steps

In 10 ml of acetone was dissolved 44.2 mg (0.1 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α;6α,7α-diepoxypregn-4-en-3-one, followed by addition of 5 mg (0.02 mmole) of pyridinium p-toluenesulfonate. The mixture was refluxed for 2 hours. The reaction mixture thus obtained was cooled to room temperature and the solvent was distilled off under reduced pressure. The residue was diluted with methylene chloride and this 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 19.6 mg of 1α,2α;6α,7α-diepoxy-3-oxopregn-4-ene-20-carbaldehyde (yield: 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112998
Source datasetuspto-grants-1992_05
ORD IDord-90c65a0f28dc4e67a8141a4d14e46d8b
Source noteuspto-grants-1992_05