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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425802Generated: October 26, 2026

Tetrahydrofuran → 6-Bromo-2,3'-bipyridine

https://huagongshe.com/reaction/2425802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2,6-DibromopyridineHCID 12274—
Reactant3-BromopyridineHCID 12286—
ReactantButyllithiumHCID 178418339—
CatalystDichloro(N,N,N',N'-tetramethylethylenediamine)zinc(II)HCID 86584708—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product6-Bromo-2,3'-bipyridineHCID 1354645444.7%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07964293B2
Source datasetuspto-grants-2011_06
ORD IDord-f8478495cbd744ee8c9098f2ee42001d
Source noteuspto-grants-2011_06