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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-Bromo-6-(pyridin-2-yl)pyridine | HCID 11791152 | 67.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442797B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-2735ac6a69a14e95bf4c5163b9fd3526 |
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| Source note | uspto-grants-2008_10 |
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