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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 42554Generated: October 25, 2026

Water → 1-(4-Fluorophenyl)-2-(4-pyridyl)vinyl 4-fluorobenzoate

https://huagongshe.com/reaction/42554

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
Reactant1-(4-Fluorophenyl)-2-(pyridin-4-yl)ethan-1-oneHCID 10330881—
SolventDimethylformamideHCID 6228—
Product1-(4-Fluorophenyl)-2-(4-pyridyl)vinyl 4-fluorobenzoateHCID 68445862152.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of NaH (0.81 g, 18.6 mmol) in DMF (30 mL) under argon atmosphere and cooled to 0° C., a solution of 1-(4-fluorophenyl)-2-(4-pyridyl)ethanone (2.00 g, 9.3 mmol, obtained in reference example 1) in DMF (15 mL) was added and stirred to room temperature for 30 minutes. It was then cooled to 0° C. and a solution of 4-fluorobenzoyl chloride (2.95 g, 1.9 mmol) in DMF (10 mL) was added. It was stirred at room temperature overnight. Water was added and the solvent was evaporated off. The residue was dissolved in a mixture of CHCl3 and water and the phases were separated. The aqueous phase was extracted with CHCl3 (×3). The organic phase was washed with water (×2), dried over Na2SO4 and concentrated to dryness. The crude product obtained was purified by chromatography on silica gel using hexane-EtOAc mixtures of increasing polarity as eluent, to afford 0.98 g of the desired compound as a yellow solid (yield: 31%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536194B2
Source datasetuspto-grants-2013_09
ORD IDord-40e9414b27794d87b43015f35338f418
Source noteuspto-grants-2013_09