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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452355Generated: October 29, 2026

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

https://huagongshe.com/reaction/452355

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-phenyl pyridine and 40 mg (0.716 mmol) of iron powder were mixed and stirred. It was cooled to 0° C. and 4.0 g (25 mmol) of bromine was added dropwise with stirring, and watching heat generation, and it was raised to 90° C., and stirred for 10 hours. After the reaction, this reaction mixture was dissolved in chloroform to produce a solution, which was washed with 5% sodium thiosulfate aqueous solution. The chloroform solution was dried with sodium sulfate, and then concentrated. The residue was purified by silica gel column chromatography, and the desired 2-(bromophenyl)pyridine was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492007B2
Source datasetuspto-grants-2013_07
ORD IDord-7a9e177fe2674b13aa753ee058bd7e03
Source noteuspto-grants-2013_07