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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 860413Erstellt: 24. Oktober 2026

Hydrochloric Acid → Ethyl 7-(4-fluorobenzoyl)-8-oxononanoate

https://huagongshe.com/de/reaction/860413

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
EduktEthyl 6-bromohexanoateHCID 117544—
Edukt1-(4-Fluoro-phenyl)-butane-1,3-dioneHCID 432655—
KatalysatorTetrabutylammonium BromideHCID 74236—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl 7-(4-fluorobenzoyl)-8-oxononanoateHCID 57444527—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 1-(4-fluorophenyl)butane-1,3-dione (1.0 g), potassium carbonate (3.84 g), and tetrabutylammonium bromide (90 mg) in toluene (20 ml) was refluxed for 3 hours, then ethyl 6-bromohexanoate (1.18 ml) was added. After stirring at 100° C. for 3 hours, the mixture was partitoned between ethyl acetate and 0.5N hydrochloric acid. 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 7-(4-fluorobenzoyl)-8-oxononanoate (983 mg) as an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07153854B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-1b492a1ead7a4f64b5ca605ce0ca112b
Quellennotizuspto-grants-2006_12