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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356765Generated: October 30, 2026

Water → Ethyl 4-(4-chloro-3-fluorophenyl)-4-oxobutanoate

https://huagongshe.com/reaction/2356765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcrylateHCID 8821—
ReactantSodium CyanideHCID 8929—
Reactant4-Chloro-3-FluorobenzaldehydeHCID 2724985—
SolventDimethylformamideHCID 6228—
ProductEthyl 4-(4-chloro-3-fluorophenyl)-4-oxobutanoateHCID 24727751—

Reaction Steps

Under argon atmosphere, to a solution of 4-chloro-3-fluoro-benzaldehyde (10 g) in N,N-dimethylformamide (50 ml) was added sodium cyanide (620 mg) at room temperature, and the mixture was stirred at the same temperature for 3 hours. Then, to the mixture was added dropwise a solution of ethyl acrylate (5.2 ml) in N,N-dimethylformamide (25 ml), and the resulting mixture was stirred at the room temperature for 3 hours. The reaction mixture was poured into water and extracted with diethyl ether. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. The resulting residue was purified by silica gel column chromatography (solvent: hexane:ethyl acetate=20:1) to obtain ethyl 4-(4-chloro-3-fluorophenyl)-4-oxobutyrate (9.4 g) as pale yellowish powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759373B2
Source datasetuspto-grants-2010_07
ORD IDord-1bff6aff966f41ff8e7087dd95c4d335
Source noteuspto-grants-2010_07