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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 483015Erstellt: 26. Oktober 2026

Phenethyl bromide → Ethyl 3-oxo-2-(2-phenylethyl)butanoate

https://huagongshe.com/reaction/483015

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenethyl bromideHCID 7666—
EduktEthyl AcetoacetateHCID 8868—
EduktSodium MethoxideHCID 10942334—
LösungsmittelEthanolHCID 702—
ProduktEthyl 3-oxo-2-(2-phenylethyl)butanoateHCID 21945991,3%

Reaktionsschritte

Ethyl acetoacetate (53.8 g., 0.29 mole) was dissolved in 110 ml. of anhydrous ethanol. Sodium methoxide (17.3 g., 0.36 mole) was added portionwise to the stirred solution, allowing the temperature to rise to 40°-50°. The mixture was then heated to reflux (80°-82°) and phenethyl bromide (53.8 g., 0.32 mole) added dropwise over 1 hour. Reflux was continued for 20 hours. The reaction mixture was cooled to 30°-35° and filtered over diatomaceous earth with ethanol wash. The combined filtrate and wash were concentrated in vacuo to a pot temperature of 50°, cooled to 25°, diluted with 150 ml. of hexane and 40 ml. of water, acidified to pH 6.5-7.0 with 6N HCl. The hexane layer was separated and washed with 25 ml. of fresh water. The aqueous layer were combined and back-washed with 40 ml. of fresh hexane. The hexane layers were combined, washed with 60 ml. of water, dried over 15 g. MgSO4, filtered and evaporated to yield title product as an oil (62 g., 91%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04576964
Quelldatensatzuspto-grants-1986_03
ORD IDord-273244fa72cc45449396d994d0ae100d
Quellennotizuspto-grants-1986_03