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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196332Generated: November 1, 2026

Acetone → 6alpha,7alpha-Diepoxypregn-4-ene-20-carbaldehyde

https://huagongshe.com/reaction/1196332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactant6alpha,7alpha-Diepoxypregn-4-en-3beta-yl acetateHCID 86745800—
Product6alpha,7alpha-Diepoxypregn-4-ene-20-carbaldehydeHCID 8674580748%

Reaction Steps

In 5 ml of acetone was dissolved 24.3 mg (0.05 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α;6α,7α- diepoxypregn-4-en-3β-yl acetate, followed by addition of 2.5 mg (0.01 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. To the residue was added methylene chloride and the mixture 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 9.6 mg of 3β-acetoxy-1α,2α;6α,7α-diepoxypregn-4-ene-20-carbaldehyde (yield: 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112998
Source datasetuspto-grants-1992_05
ORD IDord-f60c0f8521124d9485efd4a397bdb2cc
Source noteuspto-grants-1992_05