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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196328Generated: October 31, 2026

p-Toluenesulfonic acid → 1alpha,3beta-Dihydroxypregna-5,7-diene-20-carbaldehyde

https://huagongshe.com/reaction/1196328

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant20-(5,5-Dimethyl-1,3-dioxan-2-yl)pregna-5,7-diene-1alpha,3beta-diolHCID 67852945—
SolventAcetoneHCID 180—
Product1alpha,3beta-Dihydroxypregna-5,7-diene-20-carbaldehydeHCID 5389278182%

Reaction Steps

In 10 ml of acetone was dissolved 4.3 mg (0.010 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)pregna-5,7-diene-1α,3β-diol, followed by addition of 1 ml of a 1 mmole/l solution of p-toluenesulfonic acid in acetone (containing 0.001 mmole of p-toluenesulfonic acid). 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 dissolved in 40 ml of methylene chloride and this methylene chloride solution was washed with saturated aqueous sodium hydrogen carbonate solution and saturated aqueous sodium chloride solution in that order and dried over magnesium sulfate. The solvent was distilled off under reduced pressure and the residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane=1:5, v/v) to give 2.8 mg of 1α,3β-dihydroxypregna-5,7-diene-20-carbaldehyde (yield: 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112998
Source datasetuspto-grants-1992_05
ORD IDord-739f9e4c4ae446e880c719ded225d5d5
Source noteuspto-grants-1992_05