Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45436Generated: October 26, 2026

2-Bromopyridine → 2-(3-Bromophenyl)pyridine

https://huagongshe.com/reaction/45436

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Bromophenyl)boronic acidHCID 2734318—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-(3-Bromophenyl)pyridineHCID 1111550675%

Reaction Steps

A mixture of 2-bromopyridine (4.8 g, 30.33 mmol), 3-bromophenyl boronic acid (4.06 g, 20.22 mmol), glyme (35 mL), tetrakis(triphenylphosphine)palladium(0) (0.4 g) and a solution of potassium carbonate (7.6 g, 55 mmol) in water (35 mL) was stirred well at reflux under nitrogen overnight. After cooling, the reaction mixture was diluted with ethyl acetate (600 mL) and washed with water (3×200 mL). The solvent and excess 2-bromopyridine were removed on a rotary evaporator (bath temperature=75° C.) and the crude product was purified by chromatography on silica (110 g) with 2% ethyl acetate in heptane (6 L) to produce 1 (3.55 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541522B2
Source datasetuspto-grants-2013_09
ORD IDord-7c1a895424ee4f9aa5b900cf7094252a
Source noteuspto-grants-2013_09