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
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 20-(5,5-Dimethyl-1,3-dioxan-2-yl)pregna-5,7-diene-1alpha,3beta-diol | HCID 67852945 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1alpha,3beta-Dihydroxypregna-5,7-diene-20-carbaldehyde | HCID 53892781 | 82% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05112998 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-739f9e4c4ae446e880c719ded225d5d5 |
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| Source note | uspto-grants-1992_05 |
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