HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654419Generated: November 1, 2026
Dimethylformamide → 3,3-(Ethylenedioxy)-11beta-(4-vinylphenyl)-5-estren-17-one
https://huagongshe.com/reaction/1654419
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Tri(butyl)vinyltin | HCID 53438229 | — |
| Reactant | 3,3-(Ethylenedioxy)-11beta-(4-trifluoromethylsulfonyloxyphenyl)-5-estren-17-one | HCID 86748621 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3,3-(Ethylenedioxy)-11beta-(4-vinylphenyl)-5-estren-17-one | HCID 67789045 | — |
Reaction Steps
1.7 g of 3,3-(ethylenedioxy)-11β-(4-trifluoromethylsulfonyloxyphenyl)-5-estren-17-one is dissolved in 25 ml of absolute dimethylformamide and mixed with 270 mg of lithium chloride and 190 mg of tetrakistriphenylphosphinepalladium. After five more minutes of stirring, the reaction mixture is mixed with 1.15 ml of tributylvinyltin, stirred for 1 hour at 110° C. under protective gas, cooled to room temperature and diluted with ethyl acetate. After filtration on Celite and washing of the filter residue with ethyl acetate, the organic phase is washed with saturated sodium chloride solution, dried on sodium sulfate and concentrated by evaporation in a vacuum. Chromatography of the residue on aluminum oxide (neutral, stage II) with a mixture of ethyl acetate/hexane yields 1.2 g of 3,3-(ethylenedioxy)-11β-(4-vinylphenyl)-5-estren-17-one 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-77d1da54283649fe8e0dbed8110395d4 |
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| Source note | uspto-grants-1995_04 |
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