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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506155Generated: October 25, 2026

Water → Ethyl 3-(4-fluorophenyl)acrylate

https://huagongshe.com/reaction/1506155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethyl phosphonoacetateHCID 13345—
Reactant4-FluorobenzaldehydeHCID 68023—
ReactantEthanol sodium ethoxideHCID 23706232—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(4-fluorophenyl)acrylateHCID 537305991%

Reaction Steps

4-Fluorobenzaldehyde (9.61 g, 80.0 mmol) in tetrahydrofuran (120 mL) was mixed with ethyl 2-(diethoxyphosphoryl)acetate (17.9 g, 80.0 mmol) under cooling with ice, and then sodium ethoxide-ethanol solution (21 wt %, 44.8 mL, 120 mmol) was added dropwise to the reaction mixture under cooling with ice, and the resulting reaction mixture was stirred at room temperature for 2 hours. After addition of water, the reaction mixture was extracted with ethyl acetate, and the organic layer dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=20/1→10/1 (v/v)) to give the title compound as a colorless oil (14.1 g, yield 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-a09054b200b64d068416ddf3a74431a4
Source noteuspto-grants-2015_12