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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271110Generated: November 2, 2026

Triethylamine → 4-(Phenylethynyl)pyridine

https://huagongshe.com/reaction/271110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenylacetyleneHCID 10821—
Reactant4-Bromopyridinium chlorideHCID 88100—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product4-(Phenylethynyl)pyridineHCID 35217291%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a suspension of 4-bromopyridine hydrochloride (3.9 g, 20 mmol), tetrakis(triphenylphosphine)palladium (2.32 g, 2.0 mmol), triethylamine (16.8 mL, 120 mmol) in dry DMF (150 mL) is added phenylacetylene (4.2 mL, 40 mmol) at room temperature. After stirring for 3 hours at 80° C., the reaction mixture is concentrated. The residue is dissolved in CH2Cl2 (100 mL), washed with H2O, brine (50 mL), dried (MgSO4) and concentrated. The crude material is purified by chromatography (silica gel, EtOAc/hexane: 10/90) to afford the title compound as a solid (3.25 g, 91%). Mp 51-53° C. MS (+) ES: 180 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452885B2
Source datasetuspto-grants-2008_11
ORD IDord-9aaebb51c18c4dbfa6675e1f33750886
Source noteuspto-grants-2008_11