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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 860412Erstellt: 24. Oktober 2026

Hydrochloric Acid → Ethyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoate

https://huagongshe.com/de/reaction/860412

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-Fluorobenzoyl chlorideHCID 67879—
EduktEthyl 3-oxo-4-phenylbutanoateHCID 225855—
EduktMagnesium ChlorideHCID 5360315—
LösungsmittelPyridineHCID 1049—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoateHCID 5744452567,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a suspensin of magnesium chloride (1.46 g) in tetrahydrofuran (10 ml) was added a solution of ethyl 3-oxo-4-phenylbutanoate (2.0 g) in tetrahydrofuran (10 ml) and the mixture was cooled to 0° C., then pyridine (2.5 ml) was added. The mixture was stirred at 20° C. for 30 minutes, then a solution of 4-fluorobenzoyl chloride (2.44 g) in tetrahydrofuran (10 ml) was added at 0° C. After stirring at 20° C. for 2 hours, the mixure was partitoned between 0.5N hydrochloric acid and ethyl acetate. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:5) to give ethyl 2-(4-fluorobenzoyl)-3-oxo-4-phenylbutanoate (2.15 g) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07153854B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-6e2cc6132f9e4460b2e12f9e04928393
Quellennotizuspto-grants-2006_12