Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | (15α)-13-Ethyl-15-hydroxygon-4-ene-3,17-dione | HCID 15513180 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 67362260 | HCID 67362260 | — |
Reaction Steps
At 0° C., 77.5 ml of methanesulfonyl chloride is added dropwise within 10 minutes to 250 g of 15α-hydroxy-18-methyl-4-estrene-3,17-dione in 704 ml of pyridine. After 3.5 hours, 350 ml of dimethylformamide and 283 g of anhydrous sodium acetate are added, the mixture is stirred under argon for 20 hours at room temperature, and the reaction mixture is introduced into ice water. The thus-precipitated product is suctioned off, washed with water, and dried under vacuum. For purposes of purification, the crude product (212 g) is treated with 21 g of active carbon in 1,500 ml of ethyl acetate and 0.4 ml of pyridine. After concentrating the solution to 420 ml, 188 g of 18-methyl-4,15-estradiene-3,17-dione is crystallized at 0° C. Melting point 156.9° C. (from acetone/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04719054 |
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| Source dataset | uspto-grants-1988_01 |
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| ORD ID | ord-da1ba72222da460d9b4c312404246c14 |
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| Source note | uspto-grants-1988_01 |
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