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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64706Erstellt: 24. Oktober 2026

N,N-Dimethylaniline → 16beta-Ethyl-17beta-(2-bromo-2-methylpropionyloxy)4-estren-3-one

https://huagongshe.com/de/reaction/64706

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-DimethylanilineHCID 949—
EduktEthyl AcetateHCID 8857—
Edukt2-Bromo-2-methylpropionyl bromideHCID 88685—
EduktOxendoloneHCID 443947—
LösungsmittelDichloromethaneHCID 6344—
Produkt16beta-Ethyl-17beta-(2-bromo-2-methylpropionyloxy)4-estren-3-oneHCID 70467305—

Reaktionsschritte

In 30 ml of dichloromethane are dissolved 3.2 g of 16β-ethyl-17β-hydroxy-4-estren-3-one and 1.2 ml of dimethylaniline and, with stirring at room temperature (15°-25° C.), 1.0 ml of 2-bromo-2-methylpropionyl bromide is added to the above solution. The mixture is stirred at room temperature (15°-25° C.) for 16 hours, followed by addition of 300 ml of ethyl acetate. The mixture is washed with 10% phosphoric acid, water, 5% aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride in that order and dried over anhydrous magnesium sulfate. The solvent is then distilled off under reduced pressure and the residue is subjected to column chromatography. Following passage of 400 ml of diisopropyl ether-n-hexane (1:1), elution is carried out with 800 ml of the same solvent system. The eluate is evaporated under reduced pressure to remove the solvent, giving 2.6 g of the above-identified compound as a light-yellow viscous oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04609650
Quelldatensatzuspto-grants-1986_09
ORD IDord-21598c1f3df748a9a17a46da1a1ea233
Quellennotizuspto-grants-1986_09