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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217599Generated: October 29, 2026

2,5-Dibromopyridine → 5-Bromo-2-(3-methoxy-prop-1-ynyl)-pyridine

https://huagongshe.com/reaction/217599

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DibromopyridineHCID 69353—
Reactant3-MethoxypropyneHCID 69393—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-2-(3-methoxy-prop-1-ynyl)-pyridineHCID 2250326159.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 2,5-dibromo-pyridine (41, 4.64 g, 19.6 mmol), 3-methoxy-propyne (30, 1.66 mL, 19.7 mmol), and copper(I) iodide (0.084 g, 0.44 mmol) in 61.6 mL of triethylamine was purged with nitrogen, and bis(triphenylphosphine)palladium(II) chloride (0.31 g, 0.44 mmol) was added at 0° C. The resulting mixture was stirred at 0° C. for 1 hour, then at room temperature for 1 hour. The reaction mixture was diluted with ethyl acetate, then washed with water and brine. The organic layer was dried with anhydrous sodium sulfate, filtered and the filtrate concentrated under vacuum. The crude material was purified by silica gel flash chromatography eluting with ethyl acetate and hexane. The appropriate fractions were combined and the solvents removed under vacuum to provide the desired compound (42, 2.64 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198273B2
Source datasetuspto-grants-2012_06
ORD IDord-e3b5e0cbec874752834aaf1c6e5f504c
Source noteuspto-grants-2012_06