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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 592238Erstellt: 25. Oktober 2026

Toluene → 4-(4-Bromo-2-fluorophenyl)-2-fluoropyridine

https://huagongshe.com/reaction/592238

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktSodium CarbonateHCID 10340—
Edukt4-Bromo-2-fluoro-1-iodobenzeneHCID 2724516—
Edukt2-Fluoropyridine-4-boronic acidHCID 2783396—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt4-(4-Bromo-2-fluorophenyl)-2-fluoropyridineHCID 58447799—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To a sealed tube were added 4-bromo-2-fluoro-1-iodobenzene 207-1 (600 mg, 2.0 mmol), 2-fluoropyridin-4-ylboronic acid 205-4 (282 mg, 2.0 mmol), Pd(PPh3)4 (116 mg, 0.1 mmol), Na2CO3 (636 mg, 6.0 mmol), toluene (2 mL), H2O (2 mL) and ethanol (0.5 mL). The reaction mixture was stirred at 120° C. overnight. After cooling to room temperature, the solvents were evaporated and the residue was redissolved in water (5 ml) and extracted with ethyl acetate (8 mL×3). The combined organic phases were dried over Na2SO4, and concentrated. The residue was purified by silica gel flash chromatography and eluted with 15% ethyl acetate in hexane to give 4-(4-bromo-2-fluorophenyl)-2-fluoropyridine 207-3. MS m/z 270.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09238646B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-790d60a35e7749fea67bc5c6d6d3c851
Quellennotizuspto-grants-2016_01