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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879082Generated: October 25, 2026

Sodium Carbonate → 2',4'-Dichloro-4-ethylbiphenyl-3-carbaldehyde

https://huagongshe.com/reaction/879082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant(2,4-Dichlorophenyl)boronic acidHCID 2734659—
Reactant5-Bromo-2-ethylbenzaldehydeHCID 54772389—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2',4'-Dichloro-4-ethylbiphenyl-3-carbaldehydeHCID 86663674—

Reaction Steps

A suspension of 5-bromo-2-ethylbenzaldehyde (1.0 g, 4.7 mmol), 2,4-dichlorophenyl boronic acid (1.34 g, 7.0 mmol) and sodium carbonate (0.99 g, 7.98 mmol) in a mixed solvent system of 1,2-dimethoxyethane (12 ml) and distilled water (4 ml) is stirred under a nitrogen atmosphere, then flushed with nitrogen (×2). [1,1′-Bis(diphenylphosphino)ferrocene]palladium(II)chloride (1.15 g, 1.41 mmol) is then added in one portion and the suspension is again flushed with nitrogen, then heated at reflux overnight. After cooling to room temperature the reaction mixture is diluted with distilled water (10 ml) and extracted with dichloromethane (10 ml). The aqueous phase is extracted again with dichloromethane (×2), and the combined organic fractions are finally washed with brine then dried over magnesium sulfate. The crude product is purified by flash column chromatography (isohexane to 75:25 isohexane/ethyl acetate ratio eluant) to afford 2′,4′-dichloro-4-ethylbiphenyl-3-carbaldehyde as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987476B2
Source datasetuspto-grants-2015_03
ORD IDord-1d18297f608e4ff4afed1060131c0dba
Source noteuspto-grants-2015_03