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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121314Generated: November 4, 2026

2-Phenylpyridine → 2-(2-Bromophenyl)pyridine

https://huagongshe.com/reaction/2121314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenylpyridineHCID 13887—
ReactantBromineHCID 24408—
CatalystIronHCID 23925—
SolventChloroformHCID 6212—
Product2-(2-Bromophenyl)pyridineHCID 1322392935.4%

Reaction Conditions

Temperature90 °C

Reaction Steps

2-Phenylpyridine 3 g(19.3 mmol) and iron powder 40 mg(0.716 mmol) were mixed and stirred. Bromine 4.0 g (25 mmol) was added dropwise with stirring at 0° C., avoiding the rising temperature. Then the mixture was heated up to 90° C. and keep the temperature for ten hours with stirring. After the completion of the reaction, this reaction mixture was dissolved into chloroform solution and washed with 5% aqueous sodium thiosulfate solution. After dried by sodium sulufate, the organic solution was concentrated by an evaporator. The residue obtainedwas purifiedbyuse of silica gel column chromatography. 1.6 g (6.83 mmol) of 2-(bromophenyl)pyridine was obtained and the yield was 35.4%. Analysis: M+=234.0 By FD-MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696180B2
Source datasetuspto-grants-2004_02
ORD IDord-2e2663cb402a498e9c71ffccaeb94064
Source noteuspto-grants-2004_02