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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606805Generated: October 31, 2026

Triethylamine → 3-Bromo-5-(4-fluorophenylethynyl)-pyridine

https://huagongshe.com/reaction/606805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-FluoroiodobenzeneHCID 9605—
Reactant3-Bromo-5-ethynylpyridineHCID 15423879—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product3-Bromo-5-(4-fluorophenylethynyl)-pyridineHCID 67047615—

Reaction Conditions

Temperature50 °C

Reaction Steps

Sequentially add triethylamine (161 mL, 1156 mmol), bis(triphenylphosphine)palladium(II) dichloride (2 g, 2.89 mmol) and copper (I) iodide (1.1 g, 5.78 mmol) to a solution of 3-bromo-5-ethynylpyridine (52.7 g, 289 mmol), (prepared essentially as described in PREPARATION 23), and 1-fluoro-4-iodobenzene (58.4 g, 262.7 mmol) in acetonitrile (1000 mL). Purge the system with nitrogen and heat the reaction mixture at 50° C. for 16 h. Concentrate, dissolve the residue in 10:1 hexanes:dichloromethane (1000 mL), filter and concentrate. Stir the residue in 150 mL of hexanes at room temperature for 30 min to produce a slurry. Cool the slurry at 0° C. and filter to give the title compound. From the filtrate, a second crop of the title compound can be isolated (45.5 g, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915424B2
Source datasetuspto-grants-2011_03
ORD IDord-cdc7a2a585d74177986bb50678d97159
Source noteuspto-grants-2011_03