Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 4-Methoxybenzenethiol | HCID 12765 | — |
| Reactant | HCID 13421116 | HCID 13421116 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 88684209 | HCID 88684209 | — |
Reaction Steps
To a solution of 9-fluoro-11β-hydroxyandrosta-1,4-diene-3,17-dione (3.18 g) in a mixture of dry dichloromethane (40 ml) and glacial acetic acid (40 ml) containing p-methoxybenzenethiol (5.6 g) is added boron trifluoride etherate (3.0 ml) and the resulting solution is stirred for 1.5 hours. It is then poured into water (500 ml) and extracted with chloroform. The chloroform extracts are combined, washed with saturated sodium bicarbonate solution and water, dried (MgSO4) and concentrated in vacuo to a syrupy residue. This is absorbed on a column of silica gel (50 g) made up in chloroform-hexane (1:1) and the column is eluted successively with chloroform-hexane (1:1), chloroform and chloroform-ethyl acetate mixtures (95:5 and 90:10) to elute successively p-methoxybenzenethiol contaminated with some steroidal impurities, the title compound (3.0 g), a small amount of an undentified compound and unreacted starting material (1.0 g). The 3.0 g of material is refluxed with ethyl acetate (30 ml), cooled and filtered to leave the analytical specimen (dried at 0.3 mm of Hg, 100° C., 18 hours) of the title compound (2.8 g), melting point 209°-211° C., with consistent spectral data.
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-2f1d7825931d42bb8adad7bd0633718c |
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| Source note | uspto-grants-1982_11 |
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