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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 241423Erstellt: 26. Oktober 2026

Sodium Carbonate → 5-Chloro-3'-phenyl-2-methylbiphenyl

https://huagongshe.com/reaction/241423

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt2-Bromo-4-chloro-1-methylbenzeneHCID 609898—
Edukt(3-Phenylphenyl)boronic acidHCID 2734315—
KatalysatorTrioctylmethylammonium chlorideHCID 21218—
LösungsmittelTolueneHCID 1140—
Produkt5-Chloro-3'-phenyl-2-methylbiphenylHCID 6708649077%

Reaktionsschritte

To a 2 L round bottle flask equipped with reflux condenser, stir bar, nitrogen feed, and oil bath were added 2-bromo-4-chlorotoluene (20.67 g, 98.59 mmol), 3-biphenylboronic acid (20.50 g 103.52 mmol), sodium carbonate (158 mL, 315 mmol), Aliquat 336 (4.00 g) and toluene (600 mL). Solution was purged with nitrogen for 20 minutes before adding tetrakis(triphenylphospine)palladium(0) (1.14 g, 0.98 mmol) and purged for another 10 minute. The reaction was then heated under nitrogen for 18 hour. After cooing to ambient temperature, the organic phase was separated, washed with 10% HCl (200 mL), water (200 mL) and saturated brine (200 mL). This solution was dried with magnesium sulfate (50 g) for 3 hour and the solvent was removed by rotary evaporation. The crude product was filtered, washing with hexane. Product containing fractions were identified by UPLC and collected. Low boiling point is impurities and solvents were removed by Kruger-Rohr distillation to give the product as colorless oil (20.2 g, 77%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08648333B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-289fa374ccec4861ae43e9f8f42b1f9b
Quellennotizuspto-grants-2014_02