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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441489Generated: November 1, 2026

Tetrahydrofuran → 5-Bromo-2-cyclopropylpyridine

https://huagongshe.com/reaction/1441489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2,5-DibromopyridineHCID 69353—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178418630HCID 178418630—
CatalystPalladium ChlorideHCID 24290—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystZincchlorideHCID 3007855—
Product5-Bromo-2-cyclopropylpyridineHCID 2231772250%

Reaction Steps

0.5M Zinc chloride in THF (5.5 mL, 2.8 mmol) was added to a solution of 0.5M cyclopropylmagnesium bromide in THF (5.5 mL, 2.8 mmol) under argon. The solution was stirred at RT for 2 h at which time a slurry had formed. To this slurry was added in one portion 2,5-dibromopyridine (0.65 g, 2.8 mmol) and PdCl2×dppf (0.041 g, 0.050 mmol). After a few minutes an exotherm was seen and the slurry became thicker, the exotherm subsided and the slurry was stirred at RT overnight. The reaction mixture was poured into saturated sodium bicarbonate solution and extracted with ether. The ether phase was dried, filtered and concentrated, then re-dissolved in DCM and applied to a short plug of silica gel. The gel was washed with DCM and the washings were concentrated. The residue was taken up in ether and washed with 1.0M hydrochloric acid. The acidic water phase was made basic with 2.0M sodium hydroxide and the product was extracted back into ether. The combined ether phases were washed with brine, dried, filtered and concentrated to give 0.28 g (50%) of 5-bromo-2-cyclopropylpyridine as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655664B2
Source datasetuspto-grants-2010_02
ORD IDord-1aa52efa1a4947a2882f743a4a691963
Source noteuspto-grants-2010_02