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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 860413Generated: October 25, 2026

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

https://huagongshe.com/reaction/860413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 6-bromohexanoateHCID 117544—
Reactant1-(4-Fluoro-phenyl)-butane-1,3-dioneHCID 432655—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductEthyl 7-(4-fluorobenzoyl)-8-oxononanoateHCID 57444527—

Reaction Conditions

Temperature100 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07153854B2
Source datasetuspto-grants-2006_12
ORD IDord-1b492a1ead7a4f64b5ca605ce0ca112b
Source noteuspto-grants-2006_12