Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86748619 | HCID 86748619 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 9821134 | HCID 9821134 | — |
Reaction Steps
17,17-bis-(ethylenedioxy)-11β-(4-methoxyphenyl)-5-estrene is dissolved in 50 ml of acetone and mixed under protective gas with 2.5 ml of 4 n aqueous hydrochloric acid. After three hours of stirring at room temperature and one hour at 40° C., the reaction mixture is poured on cold saturated sodium bicarbonate solution and the aqueous phase is extracted several times with methylene chloride. The combined organic phases are dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue is chromatographed on silica gel-with a mixture of ethyl acetate/hexane. 683 mg of 11β-(4-methoxyphenyl)-4-estrene-3,17-dione is obtained as white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05405979 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-f9f13df5336a491ebf11eef47c933d68 |
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| Source note | uspto-grants-1995_04 |
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