HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 70464278, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 13421116 | HCID 13421116 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 70464278 | HCID 70464278 | — |
Reaction Steps
A solution of 20 g of 9-fluoro-11β-hydroxyandrosta-1,4-diene-3,17-dione, 120 ml of glacial acetic acid, 120 ml of acetic anhydride and 5 g of p-toluenesulfonic acid is stirred at room temperature under nitrogen for 24 hours. The resulting solution is quenched with 5 g of sodium acetate. The solvent is partially removed in vacuo at 35°-40° C. and the resultant slurry is diluted with chloroform. The chloroform solution is washed with water, saturated sodium bicarbonate and water, dried over anhydrous Na2SO4 and evaporated in vacuo to give the title compound. This is crystallized from ethyl acetate-hexane to give 20 g of the title compound melting point 171°-174° C., with consistent spectral data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04361559 |
| Source dataset | uspto-grants-1982_11 |
| ORD ID | ord-8f36a6ffc6a84c99a2dd12b79690a044 |
| Source note | uspto-grants-1982_11 |