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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672630Generated: November 1, 2026

Triethylamine → E-5-Fluoro-2-[2-(4-methoxyphenyl)vinyl]benzaldehyde

https://huagongshe.com/reaction/1672630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-MethoxystyreneHCID 12507—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant2-Bromo-5-fluorobenzaldehydeHCID 2773321—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductE-5-Fluoro-2-[2-(4-methoxyphenyl)vinyl]benzaldehydeHCID 5783134161.7%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 10 g (49.26 mmol) of 2-bromo-5-fluorobenzaldehyde in 200 ml of dry DMF is mixed with 7.27 g (54.18 mmol) of 4-methoxystyrene, 1.5 g (4.93 mmol) of tri-2-tolylphosphine, 330 mg (1.48 mmol) of palladium(II) acetate and 10.3 ml (73.89 mmol) of triethylamine under argon and stirred at 100° C. for 12 hours. After reaction is complete, the reaction solution is cooled to room temperature and concentrated to dryness. The resulting residue is taken up in 100 ml of water and extracted three times with 50 ml of diethyl ether each time. The combined organic phases are dried over sodium sulfate. After filtration, the solution is concentrated to dryness, and the residue is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 10:1). 7.79 g (55% yield) of a colorless solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998988B2
Source datasetuspto-grants-2011_08
ORD IDord-b7534bb800864722a5100566d95dfcbb
Source noteuspto-grants-2011_08