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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639938Generated: October 26, 2026

2-Bromopyridine → 2-(2-Chloro-phenyl)pyridine

https://huagongshe.com/reaction/1639938

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chlorophenylboronic acidHCID 2734322—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTetrahydrofuranHCID 8028—
Product2-(2-Chloro-phenyl)pyridineHCID 1114818550%

Reaction Conditions

Temperature80 °C

Reaction Steps

This Example was carried out in the same manner as Example 1, except that 5.0 g (0.032 mol) of 2-chloro-phenyl boronic acid, 10.0 g (0.064 mol) of 2-bromopyridine, 150□ of tetrahydrofuran and 2M potassium carbonate solution (20□) were added and then 0.37 g (3 mol %) of palladium tetrakistriphenylphosphine [(pd(PPh3)4] was used as a catalyst. Finally, after the resulting solution was heated to reflux at 80° C. for 24 hours, the 2-(2-chloro-phenyl)pyridine was isolated. The yield was 50%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110642B2
Source datasetuspto-grants-2012_02
ORD IDord-2fc9e8afa25b43469613e1853d778466
Source noteuspto-grants-2012_02