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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2117807Generated: October 31, 2026

2-Bromopyridine → 2-Bromo-6-(pyridin-2-yl)pyridine

https://huagongshe.com/reaction/2117807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant2,6-DibromopyridineHCID 12274—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2-Bromo-6-(pyridin-2-yl)pyridineHCID 1179115267.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a nitrogen atmosphere, a THF (5 ml) solution of bromopyridine (0.5 g) was cooled to −78° C., then a hexane solution of n-butyllithium (1.57 M, 2 ml) was added dropwise thereto, after dropwise, the mixture was stirred at 0° C. for 3 hours. Thereafter, a THF solution of zinc chloride (3.15 g) was added dropwise to the mixture, after dropwise, the mixture was stirred for 3 hours. Next, 2,6-dibromopyridine (0.75 g) and tetrakis(triphenylphosphine)palladium (146 mg) were added to the mixture at room temperature, and the mixture was refluxed for 1 day. After the reaction mixture was allowed to cool, to which was then added water, the mixture was extracted with toluene, the solvent was distilled off, and the residue was purified by silica gel column chromatography, thereby obtaining desired compound as white crystal (0.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442797B2
Source datasetuspto-grants-2008_10
ORD IDord-2735ac6a69a14e95bf4c5163b9fd3526
Source noteuspto-grants-2008_10