Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | HCID 70046766 | HCID 70046766 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Methanesulfonyl chloride | HCID 31297 | — |
| Product | HCID 70445983 | HCID 70445983 | — |
Reaction Steps
2.6 ml of a solution of 5% by weight sulphur dioxide in methanesulphonic acid chloride are added to a solution of 1.75 g of 3β-acetoxy-11β-hydroxy-15β,16β-methyleneandrost-5-en-17-one in 10.5 ml of dimethylformamide and 3.5 ml of γ-collidine and the whole is stirred for 20 minutes, the internal temperature being allowed to rise to approximately 45°. While stirring, the mixture, including the precipitate that has formed, is poured onto 17.5 ml of ice-water and stirring is continued for a further 10 minutes. The oil that separates out is taken up in ethyl acetate and washed in succession with saturated sodium chloride solution, ice-cold dilute hydrochloric acid, ice-cold dilute sodium hydroxide solution and again with saturated sodium chloride solution. Evaporation of the solvent yields 3β-acetoxy-15β,16β-methyleneandrosta-5,9(11)-dien-17-one that is uniform according to thin-layer chromatography and is processed further without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04670551 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-fa28453fde0548c5b20f83e61a8adbd1 |
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| Source note | uspto-grants-1987_06 |
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