HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154781Generated: October 31, 2026
Hydrochloric Acid → 16-Ethylidene-3-methoxy-1,3,5(10)-estratrien-17-one
https://huagongshe.com/reaction/1154781
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 16-Dimethylaminomethylene-3-methoxy-1,3,5(10)-estratrien-17-one | HCID 54161361 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 16-Ethylidene-3-methoxy-1,3,5(10)-estratrien-17-one | HCID 54221529 | — |
Reaction Steps
A solution of 5 g. of 16-dimethylaminomethylene-3-methoxy-1,3,5(10)-estratrien-17-one in 150 ml. of toluene is combined dropwise at -10° C. with 28.5 ml. of a 5% solution of methyllithium in ether. After this dropwise addition, the mixture is agitated for 15 minutes at -10° C.; then about 10 ml. of water is gently added in drops, and the reaction solution is poured into about 200 ml. of 0.5 N hydrochloric acid. The organic phase is separated, dried over sodium sulfate, and concentrated under vacuum. After crystallization of the residue from ethyl acetate/ether, 3.9 g. of 16-ethylidene-3-methoxy-1,3,5(10)-estratrien-17-one is obtained, m.p. 139°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04298538 |
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| Source dataset | uspto-grants-1981_11 |
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| ORD ID | ord-3d1d44b2e1854f22b52cd720250ac87d |
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| Source note | uspto-grants-1981_11 |
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