HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271110Generated: November 2, 2026
Triethylamine → 4-(Phenylethynyl)pyridine
https://huagongshe.com/reaction/271110
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | 4-Bromopyridinium chloride | HCID 88100 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Phenylethynyl)pyridine | HCID 352172 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07452885B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-9aaebb51c18c4dbfa6675e1f33750886 |
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| Source note | uspto-grants-2008_11 |
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