HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221179Generated: October 26, 2026
Tetrahydrofuran → 6-Bromo-2,3'-bipyridine
https://huagongshe.com/reaction/221179
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Dichloro(N,N,N',N'-tetramethylethylenediamine)zinc(II) | HCID 86584708 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 6-Bromo-2,3'-bipyridine | HCID 13546454 | 44.7% |
Reaction Steps
Under nitrogen atmosphere, 6.32 g of 3-bromopyridine was dissolved in 400 ml of dehydrated toluene. The solution was cooled at −78° C. and 17 ml of 2.6M normal-butyllithium was dropped. After 0.5 hours, 12.6 g of zinc chloride tetramethylethylenediamine, and 200 ml of dehydrated THF were added. The solution was heated to room temperature, 10.63 g of 2,6-dibromopyridine and 0.6 g of Pd(PPh3)4 were added, and the solution was stirred for 24 hours. The reaction liquid was washed by an ammonium chloride aqueous solution, and the organic layer was concentrated in an evaporator. The concentrates were purified by column chromatography, and thus 4.2 g of 6-bromo-2,3′-bipyridine was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202633B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-fa783822116942fe8bc4a2cbd7be8b58 |
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| Source note | uspto-grants-2012_06 |
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