HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912882Generated: October 26, 2026
Triethylamine → 4-(4-Nitro-2-(trifluoromethyl)phenylethynyl)pyridine
https://huagongshe.com/reaction/1912882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromo-5-nitrobenzotrifluoride | HCID 136198 | — |
| Reactant | 4-Ethynylpyridine | HCID 642801 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Nitro-2-(trifluoromethyl)phenylethynyl)pyridine | HCID 23155274 | — |
Reaction Steps
In 20 mL of dimethylformamide, 1.0 g (3.7 mmol) of 4-bromo-3-(trifluoromethyl)nitrobenzene was dissolved, and 0.502 g (3.7 mmol) of 4-ethynylpyridine, 43 mg (3 mol %) of copper iodide, 78 mg (3 mol %) of dichlorobis(triphenylphosphine)palladium and 2.06 mL (0.56 mmol) of triethylamine were added thereto and the mixture solution was stirred overnight at 50° C. in an argon atmosphere. The reaction solution was partitioned between water and ethyl acetate and the organic layer was washed with a saturated sodium chloride solution and concentrated under reduced pressure. The residue was purified by a silica gel column (n-hexane:ethyl acetate=3:1) to obtain 1.3 g (quantitative) of a target product as an pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609656B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-178350c2f3cf4c4ebf09de628cdceeb6 |
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| Source note | uspto-grants-2013_12 |
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