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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415289Generated: October 29, 2026

2-Bromopyridine → 3-(Pyridin-2-yl)benzoic acid

https://huagongshe.com/reaction/415289

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Carboxyphenylboronic acidHCID 2733957—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-(Pyridin-2-yl)benzoic acidHCID 515259285%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-boronobenzoic acid (1.66 g, 10 mmol) and 2-bromopyridine (1.72 g, 11 mmol) in acetonitrile (40 mL) and water (40 mL), potassium carbonate (5.5 g, 40 mmol), Bis(triphenylphosphine)palladium(II)chloride (400 mg, 0.37 mmol) was added. The mixture was degassed and purged withed nitrogen. The mixture was stirred at 100° C. for 24 h. Then the hot suspension was filtered and concentrated to half of the original volume and washed with dichloromethane. The aquatic phase was adjusted to pH=3 with hydrochloric acid (1 M) and filtrated, washed with water. The residue was dried in vacuum to obtain 1.69 g of white solid of 3-(pyridin-2-yl)benzoic acid. Yield: 85%. LC-MS (ESI) m/z: 200 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088760B2
Source datasetuspto-grants-2012_01
ORD IDord-6069d7e6b68943bebcc42529e55df792
Source noteuspto-grants-2012_01