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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt2-Fluoropyridine-3-boronic acidHCID 2783270—
Edukt((3-Bromophenyl)ethynyl)trimethylsilaneHCID 3683324—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt2-Fluoro-3-{3-[(trimethylsilyl)ethynyl]phenyl}pyridineHCID 6870158792,8%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07705030B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-4b3c217f41ab446ba3f4c2cdb1c4c294
Quellennotizuspto-grants-2010_04