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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355624Generated: November 3, 2026

Ethanol → Sodium 4-(pyridin-4-yl)benzoate

https://huagongshe.com/reaction/1355624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant4-Chloropyridine hydrochlorideHCID 81852—
Reactant4-Carboxyphenylboronic AcidHCID 312183—
Catalyst(Butane-1,4-diyl)bis(diphenylphosphane)--dichloropalladium (1/1)HCID 10974057—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductSodium 4-(pyridin-4-yl)benzoateHCID 2367350741%

Reaction Steps

A solution of 4-chloropyridine hydrochloride (3.00 g, 20.0 mmol), 4-carboxybenzeneboronic acid (4.97 g, 30.0 mmol), 1 M aqueous sodium carbonate solution (50 mL), 1,4-bis(diphenylphosphino)butane palladium(II) dichloride (300 mg, 0.70 mmol), and ethanol (10 mL) in toluene (40 mL) was heated at reflux for 16 h. The mixture was diluted with methanol and filtered through diatomaceous earth. The filtrate was concentrated in vacuo and the pH was adjusted to 14 by the addition of 1 N aqueous sodium hydroxide. After heating the filtrate to boiling, the insoluble material was removed by filtration, and the resulting filtrate was allowed to cool to room temperature. The resulting precipitate was collected by filtration to yield 1.83 g (41%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586459B2
Source datasetuspto-grants-2003_07
ORD IDord-ba05d502b9794aa78e170e390b2ab3e1
Source noteuspto-grants-2003_07