HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17104Generated: October 25, 2026
Triethylamine → 3-Fluoro-5-((trimethylsilyl)ethynyl)benzonitrile
https://huagongshe.com/reaction/17104
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 3-Bromo-5-fluorobenzonitrile | HCID 2783330 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Fluoro-5-((trimethylsilyl)ethynyl)benzonitrile | HCID 16737211 | — |
Reaction Steps
A solution of 3-bromo-5-fluorobenzonitrile (2.5 g, 12.5 mmol), (trimethylsilyl)acetylene (2.86 ml, 20 mmol), bis(acetate)bis(triphenylphoshpino) Palladium(II) (936 mg, 1.25 mmol) and triethylamine (35 ml) in toluene (35 ml) was 15 degassed by bubbling nitrogen through the solution and then stirred at 95° C. for 30 minutes. Filtration and concentration to yield a crude product. It was diluted with EtOAc (150 ml). The organic phase was washed with saturated NaHCO3 solution (50 ml), brine (50 ml) and the organic layer was dried over sodium sulfate. Filtration and concentration to yield a product A293.1 (2.4 g, 88%). HPLC: 95%, retention time: 4.05 minute (condition A). LC/MS (M+H)+=218.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737279B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-bd280274d3164bc1abeaa913cf194cbf |
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| Source note | uspto-grants-2010_06 |
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