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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantLithium ChlorideHCID 433294—
ReactantTri(butyl)vinyltinHCID 53438229—
Reactant3,3-(Ethylenedioxy)-11beta-(4-trifluoromethylsulfonyloxyphenyl)-5-estren-17-oneHCID 86748621—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
Product3,3-(Ethylenedioxy)-11beta-(4-vinylphenyl)-5-estren-17-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405979
Source datasetuspto-grants-1995_04
ORD IDord-77d1da54283649fe8e0dbed8110395d4
Source noteuspto-grants-1995_04