HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199082Generated: October 29, 2026
p-Toluenesulfonic acid → HCID 70464278, compound
https://huagongshe.com/reaction/2199082
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 13421116 | HCID 13421116 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | HCID 70464278 | HCID 70464278 | 88.3% |
Reaction Steps
A solution of 9-fluoro-11β-hydroxyandrosta-1,4-diene-3,17-dione (5.0 g) in a mixture of acetic acid (60 ml) and acetic anhydride (60 ml) containing p-toluenesulfonic acid (2.5 g) is maintained at room temperature for eighteen hours. Sodium acetate (2.5 g) is added and the mixture is concentrated in vacuo at 35°-40° C. The residue is diluted with water (150 ml) and the solid that separates is isolated by filtration, washed with water and dried in vacuo to afford the title compound as a solid (5.0 g) with consistent spectral data. An examination (silica gel, chloroform: ethyl acetate, 95:5) reveals the presence of a small amount of starting steroid as the only significant impurity. This material is used without purification in the next step. A specimen crystallized from acetone-hexane melts at 173°-174° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04361559 |
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| Source dataset | uspto-grants-1982_11 |
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| ORD ID | ord-13a9bb9088704e3e8cfda21da5780cf1 |
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| Source note | uspto-grants-1982_11 |
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