HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106834Generated: October 30, 2026
Triethylamine → Tert-butyl 4-[2-(4-(2-phenylethenyl)-3-pyridyl)ethynyl]benzoate
https://huagongshe.com/reaction/1106834
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tert-butyl 4-ethynylbenzoate | HCID 13965008 | — |
| Reactant | 3-Bromo-4-(2-phenylethenyl)pyridine | HCID 53931587 | — |
| Catalyst | HCID 178506583 | HCID 178506583 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 4-[2-(4-(2-phenylethenyl)-3-pyridyl)ethynyl]benzoate | HCID 54016878 | 33% |
Reaction Steps
3-Bromo-4-(2-phenylethenyl)pyridine (0.74 g, 2.9 mmol) was dissolved in DMF (1.4 ml). The solution was treated with tert-butyl 4-ethynylbenzoate (0.93 g, 4.6 mmol), copper (III) iodide (0.023 g, 0.21 mmol) and triethylamine (0.64 g, 6.3 mmol). The reaction mixture was degassed by bubbling through argon and the catalyst, bistriphenyl phosphinepalladium dichloride (0.03 g, 0.043 mmol), was added. The reaction was heated to 90-100° C. for 3 hours and then partitioned between ethyl acetate and water. The organic layer was washed with water (3×), dried (MgSO4) and evaporated. The residue was purified by chromatography (eluting with ethylacetate/hexane) to give tert-butyl 4-[2-(4-(2-phenylethenyl)-3-pyridyl)ethynyl]benzoate as a dark oil (0.36 g, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057345 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-75a8a525e6174f8c9d0c05e1e0adb425 |
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| Source note | uspto-grants-2000_05 |
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