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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610376Generated: October 31, 2026

Hydrochloric Acid → Ethyl 3-(2-fluorophenyl)-3-oxopropanoate

https://huagongshe.com/reaction/1610376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Fluorobenzoic acidHCID 9935—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 178472271HCID 178472271—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-(2-fluorophenyl)-3-oxopropanoateHCID 296342160.3%

Reaction Steps

To a solution of 2-fluorobenzoic acid (25.3 g, 181 mmol) in tetrahydrofuran (300 ml) was added 1,1′-carbonylbis-1H-imidazole (32.2 g, 198 mmol) and the mixture was stirred at room temperature for 30 min. To the reaction solution was added monoethyl malonate magnesium salt (27.1 g, 94.7 mmol) 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-(2-fluorophenyl)-3-oxopropionate (31.9 g, 84%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-9e841364890b48a89b16d06241218d1a
Source noteuspto-grants-2006_01