Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060991Generated: November 2, 2026

Hydrochloric Acid → [2,4'-Bipyridine]-5-carboxylic acid hydrochloride

https://huagongshe.com/reaction/1060991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant6-Chloronicotinic acidHCID 79222—
Reactant4-(Diethylboranyl)pyridineHCID 13318871—
ReactantPotassium hydrochlorideHCID 86590535—
CatalystTetrabutylammonium BromideHCID 74236—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product[2,4'-Bipyridine]-5-carboxylic acid hydrochlorideHCID 69483715—

Reaction Steps

In tetrahydrofuran (20 ml), 6-chloronicotinic acid (535 mg) and diethyl (4-pyridyl)borane (500 mg) were dissolved. To the resulting solution, tetrabutylammonium bromide (546 mg), potassium hydrochloride (570 mg), tetrakis(triphenylphosphine)palladium (0) (392 mg) and water (0.5 ml) were added, followed by heating under reflux for 6 hours. Dilute hydrochloric acid was added to the reaction mixture to make it acidic. Water and ethyl acetate were poured into the resulting mixture for extraction. The water layer so extracted was distilled off under reduced pressure. The residue was purified by chromatography through a synthetic adsorbent (“Diaion HP-20”, water ˜50% acetonitrile-water). To the resulting fraction, dilute hydrochloric acid was added to make it acidic. The solvent was then distilled off. Tetrahydrofuran was added to the residue and the precipitate was collected by filtration, whereby the title compound (269 mg, 32%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525042B1
Source datasetuspto-grants-2003_02
ORD IDord-6a0388fb746c4487ba703516b852bac1
Source noteuspto-grants-2003_02