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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 64727Erstellt: 24. Oktober 2026

Dimethylformamide → 16beta-Ethyl-17beta-n-heptanoyloxyacetoxy-4-estren-3-one

https://huagongshe.com/de/reaction/64727

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktHeptanoic AcidHCID 8094—
EduktSodium HydroxideHCID 14798—
Edukt16beta-Ethyl-17beta-bromoacetoxy-4-estren-3-oneHCID 15593764—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt16beta-Ethyl-17beta-n-heptanoyloxyacetoxy-4-estren-3-oneHCID 7046764664%

Reaktionsschritte

In 30 ml of acetone is dissolved 2.6 g of n-heptanoic acid, and 10 ml of 2N-NaOH, 4.2 g of 16β-ethyl-17β-bromoacetoxy-4-estren-3-one, 30 ml of DMF and 10 ml of water are serially added to the above solution. The mixture is refluxed for 5 hours. After cooling, 400 ml of ethyl acetate is added and the mixture is washed with water and saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent is then distilled off under reduced pressure and the residue is subjected to column chromatography. Following 400 ml of diisopropyl ether-n-hexane (2:3), elution is carried out with 1000 ml of a 1:1 mixture of the same solvents. The eluate is evaporated under reduced pressure to remove the solvent, giving 3.0 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-51711f58cf9043d294756a7ccce7d9b7
Quellennotizuspto-grants-1986_09