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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708761Generated: November 1, 2026

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

https://huagongshe.com/reaction/1708761

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 numberUS05359055
Source datasetuspto-grants-1994_10
ORD IDord-561fb173146b46d4be0855adfe44140c
Source noteuspto-grants-1994_10