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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610367Generated: October 30, 2026

Hydrochloric Acid → Ethyl 3-(3-fluorophenyl)-3-oxopropanoate

https://huagongshe.com/reaction/1610367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Fluorobenzoic AcidHCID 9968—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 178472271HCID 178472271—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-(3-fluorophenyl)-3-oxopropanoateHCID 2063904173.8%

Reaction Steps

To a solution of 3-fluorobenzoic acid (25.5 g, 182 mmol) in tetrahydrofuran (300 ml) was added 1,1′-carbonylbis-1H-imidazole (32.4 g, 200 mmol) and the mixture was stirred at room temperature for 30 min. Monoethyl malonate magnesium salt (27.1 g, 94.7 mmol) was added to the reaction solution and the mixture was heated under reflux for 30 min. Ethyl acetate (50 ml) and water (50 ml) were added to the reaction solution, and conc. hydrochloric acid was added until the aqueous layer showed acidic pH. The reaction solution was extracted with ethyl acetate (200 ml×2). The extract was washed with saturated brine, dried over anhydrous magnesium sulfate and evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to give ethyl 3-(3-fluorophenyl)-3-oxopropionate (34.6 g, 91%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-8b1cb3f9ed50457daf45de594cb8814f
Source noteuspto-grants-2006_01