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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708769Generated: November 3, 2026

p-Toluenesulfonic acid → 1alpha,2alpha-Epoxy-3beta,7alpha-dihydroxypregn-5-ene-20-carbaldehyde

https://huagongshe.com/reaction/1708769

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant20-(5,5-Dimethyl-1,3-dioxan-2-yl)-1alpha,2alpha-epoxypregn-5-ene-3beta,7alpha-diolHCID 86745808—
SolventAcetoneHCID 180—
Product1alpha,2alpha-Epoxy-3beta,7alpha-dihydroxypregn-5-ene-20-carbaldehydeHCID 8674581067%

Reaction Steps

In 2.5 ml of acetone was dissolved 2.2 mg (0.005 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α-epoxypregn-5-ene-3β,7α-diol, followed by addition of 0.5 ml of a 1 mmol/1 solution of p-toluenesulfonic acid in acetone (containing 0.0005 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 methylene chloride was added to the residue. This methylene chloride solution was washed successively with saturated aqueous sodium hydrogen carbonate 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 1.2 mg of 1α,2α-epoxy- 3β,7α-dihydroxypregna-5-ene-20-carbaldehyde (yield: 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05359055
Source datasetuspto-grants-1994_10
ORD IDord-1049bcfd56ee4c5ea2275c3937024b76
Source noteuspto-grants-1994_10