HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650785Generated: November 2, 2026
Water → 3-Chloromethylene-19-methylthio-4-androsten-17-one
https://huagongshe.com/reaction/1650785
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 19-Thiomethylandrost-4-ene-3,17-dione | HCID 146142 | — |
| Reactant | (Chloromethyl)triphenylphosphonium chloride | HCID 197823 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Chloromethylene-19-methylthio-4-androsten-17-one | HCID 54568467 | 49.7% |
Reaction Steps
500 mg of 19-methylthio-4-androstene-3,17-dione (European patent 100,566) is added to a suspension of 5.21 g of chloromethyl triphenylphosphonium chloride in 50 ml of tetrahydrofuran, which was stirred with 9.5 ml of (1.6 m of butyllithium in ether) 0.5 hours at 20° C., and stirred for 30 minutes at 0° C. Then it is mixed with water, extracted three times with ethyl acetate, washed neutral, dried on sodium sulfate and concentrated to dryness. 995 mg of raw product is obtained, which after chromatographic purification yields 273 mg of pure 3-chloromethylene-19-methylthio-4-androsten-17-one with a melting point of 114°-115° C., [α]D +241.5° C. (CHCl3), as pure E form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04925834 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-c2c3cbc1c3e34d9fb391d0b27f0343a3 |
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| Source note | uspto-grants-1990_05 |
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