HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75186Erstellt: 24. Oktober 2026
Triethylamine → 2-Fluoro-3-((trimethylsilyl)ethynyl)pyridine
https://huagongshe.com/de/reaction/75186
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Trimethylsilylacetylene | HCID 66111 | — |
| Edukt | 2-Fluoro-3-iodopyridine | HCID 7009501 | — |
| Katalysator | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-Fluoro-3-((trimethylsilyl)ethynyl)pyridine | HCID 53980383 | 85,9% |
Reaktionsschritte
Into a 1-neck round-bottom flask was added 2-fluoro-3-iodopyridine (1.0 g, 0.0045 mol), trimethylsilylacetylene (0.95 mL, 6.7 mmol), bis(triphenylphosphine)palladium(II) chloride (0.2 g, 0.2 mmol), copper(I) iodide (0.07 g, 0.4 mmol), and triethylamine (0.94 mL, 6.7 mmol) in N,N-dimethylformamide (20 mL). The reaction was stirred at 25° C. for 16 hours. The reaction was extracted with EtOAc, washed with brine, dried over MgSO4, and concentrated under vacuum. The product was purified by column chromatography on silica gel (10% ethyl acetate 90% hexanes) to give 0.747 g of the desired product. 1H NMR (400 MHz, CDCl3): δ 7.86-7.89 (m, 1H), 7.55-7.61 (m, 1H), 6.86-6.90 (m, 1H). MS [M+H]=194.0
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835423B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-a8e646a968b04ae98ba029057129555c |
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| Quellennotiz | uspto-grants-2014_09 |
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