HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 646222Erstellt: 24. Oktober 2026
Sodium Carbonate → 2-Fluoro-3-{3-[(trimethylsilyl)ethynyl]phenyl}pyridine
https://huagongshe.com/de/reaction/646222
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 2-Fluoropyridine-3-boronic acid | HCID 2783270 | — |
| Edukt | ((3-Bromophenyl)ethynyl)trimethylsilane | HCID 3683324 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,2-Dimethoxyethane | HCID 8071 | — |
| Produkt | 2-Fluoro-3-{3-[(trimethylsilyl)ethynyl]phenyl}pyridine | HCID 68701587 | 92,8% |
Reaktionsschritte
To a solution of [(3-bromophenyl)ethynyl](trimethyl)silane (2.28 g, 9.0 mmol) in DME (150 mL) is added (2-fluoropyridin-3-yl)boronic acid (1.41 g, 10.0 mmol), tetrakis(triphenylphosphine)palladium (0.52 g, 0.5 mmol) and a solution of sodium carbonate (3.8 g, 36.0 mmol) in H2O (15 mL) at room temperature. After refluxing for 3 h, the reaction mixture is cooled, quenched with saturated sodium carbonate, diluted with EtOAc. The two layers are separated and the aqueous layer is extracted with EtOAc. The combined organic extracts are washed with brine, dried (MgSO4) and concentrated. The crude mixture is purified by chromatography (silica gel, EtOAc/hexane:5/95) to give the 2-fluoro-3-{3-[(trimethylsilyl)ethynyl]phenyl}pyridine (2.25 g, 91%) as an oil. MS (+) APPI: 270 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07705030B2 |
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| Quelldatensatz | uspto-grants-2010_04 |
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| ORD ID | ord-4b3c217f41ab446ba3f4c2cdb1c4c294 |
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| Quellennotiz | uspto-grants-2010_04 |
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