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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550326Generated: October 30, 2026

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

https://huagongshe.com/reaction/550326

Reaction equation

Participants

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

Reaction Conditions

Temperature0 °C

Reaction Steps

3 g (19.3 mmol) of 2-phenylpyridine and 40 mg (0.716 mmol) of an iron powder were mixed and stirred. 4.0 g (25 mmol) of bromine was dropped paying attention to heat generation while stirring and cooling the mixture to 0° C., and the mixture was heated up to 90° C. and stirred for 10 hours. After completion of the reaction, this reaction mixture was dissolved in chloroform, and washed with a 5% aqueous sodium thiosulfate solution. The chloroform solution was dried over sodium sulfate, then, concentrated, and the residue was purified by silica gel column chromatography, to obtain the intended 2-(bromophenyl)pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07947340B2
Source datasetuspto-grants-2011_05
ORD IDord-66625216ddc04b3990b0170475934285
Source noteuspto-grants-2011_05