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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606929Generated: October 30, 2026

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

https://huagongshe.com/reaction/606929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-DibromopyridineHCID 69369—
Reactant1-Ethynyl-4-fluorobenzeneHCID 522627—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178419050HCID 178419050—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-5-(4-fluorophenylethynyl)-pyridineHCID 6704761551.5%

Reaction Steps

Heat a suspension of 3,5-dibromopyridine (4.00 g, 16.88 mmol), bis(triphenylphosphine)palladium (II) dichloride (0.59 g, 0.84 mmol) and copper (I) iodide (0.32 g, 1.69 mmol) in triethylamine (4.7 mL, 33.8 mmol) to 80° C. Add a solution of 1-ethynyl-4-fluorobenzene (2.03 g, 16.88 mmol) in acetonitrile (34 mL), stir for 2 h, cool to room temperature and dilute with ethyl acetate. Wash with an aqueous saturated solution of sodium bicarbonate, dry (magnesium sulfate), filter and concentrate. Purify the residue by silica gel chromatography, eluting with a 1% solution of ethyl acetate in 1:1 chloroform:hexanes, and then recrystallize from methanol to give the title compound (2.4 g, 51.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915424B2
Source datasetuspto-grants-2011_03
ORD IDord-fc0f881611404a339464bb24cd8f4f6f
Source noteuspto-grants-2011_03