HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886955Generated: October 26, 2026
Triethylamine → N-(5-Nitro-2-(phenylethynyl)phenyl)butyramide
https://huagongshe.com/reaction/1886955
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Butyramido-4-nitrophenyl trifluoromethanesulfonate | HCID 11291234 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(5-Nitro-2-(phenylethynyl)phenyl)butyramide | HCID 11358741 | 78% |
Reaction Steps
To a solution of 2-butyramido-4-nitrophenyl trifluoromethanesulfonate (860 mg, 2.42 mmol) in dry acetonitrile (30 mL) under nitrogen was added tetrabutylammonium iodide (1.34 g, 3.62 mmol), tetrakis(triphenylphosphine)palladium(0) (280 mg, 0.24 mmol) and copper iodide (140 mg, 0.72 mmol). Triethylamine (6 mL) was then added, followed by phenyl acetylene (530 μL, 4.83 mmol). The resulting solution was stirred at room temperature for 2 h. Ammonium chloride was then added to quench the reaction, and the aqueous layer was extracted with ethyl acetate. The organic layer was washed with brine. The combined organic layers were dried over anhydrous MgSO4 and evaporated. The resulting solid was purified by column chromatography eluting using a gradient (hexanes to ethyl acetate) to afford 580 mg (78%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501713B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-a4641c20fdba4c488ad1ba27e0c9b276 |
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| Source note | uspto-grants-2013_08 |
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