HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708762Generated: October 31, 2026
p-Toluenesulfonic acid → 3-Oxopregna-1,4,6-triene-20-carbaldehyde
https://huagongshe.com/reaction/1708762
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 20-(5,5-Dimethyl-1,3-dioxan-2-yl)pregna-1,4,6-trien-3-one | HCID 22843932 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Oxopregna-1,4,6-triene-20-carbaldehyde | HCID 22843885 | 75% |
Reaction Steps
In 100 ml of acetone was dissolved 0.410 g (1.0 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)pregna-1,4,6-trien-3-one, followed by addition of 10 mg (0.05 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 the residue was diluted with methylene chloride. The 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 0.243 g of 3-oxopregna-1,4,6-triene-20-carbaldehyde (yield: 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05359055 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-4987a94af035478fa2b499315b055c94 |
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| Source note | uspto-grants-1994_10 |
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