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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610494Generated: October 27, 2026

Hydrochloric Acid → Ethyl 3-(2-fluoro-4-pyridyl)-3-oxopropionate

https://huagongshe.com/reaction/1610494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-Fluoroisonicotinic acidHCID 345360—
ReactantHCID 178472271HCID 178472271—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(2-fluoro-4-pyridyl)-3-oxopropionateHCID 2226147288.9%

Reaction Steps

To a solution of 2-fluoro-4-pyridinecarboxylic acid (10 g, 70.9 mmol) in tetrahydrofuran (150 ml) was added 1,1′-carbonylbis-1H-imidazole (12.7 g, 78.0 mmol), and the mixture was heated under reflux for 30 min. The reaction solution was cooled and monoethyl malonate magnesium salt (11.2 g, 39.0 mmol) was added. The mixture was stirred at room temperature for 30 min. 1N Hydrochloric acid (200 ml) was added to the reaction solution, and the mixture 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) and recrystallized from hexane to give ethyl 3-(2-fluoro-4-pyridyl)-3-oxopropionate (7.32 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982348B2
Source datasetuspto-grants-2006_01
ORD IDord-ab864b988d2c4f138a755e23253dba79
Source noteuspto-grants-2006_01