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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1619625Erstellt: 25. Oktober 2026

Toluene → 4-(5-Chloro-2-methoxyphenyl)pyridazine

https://huagongshe.com/reaction/1619625

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktSodium CarbonateHCID 10340—
Edukt5-Chloro-2-methoxyphenylboronic acidHCID 2735751—
Edukt4-Bromopyridazine hydrobromideHCID 53407906—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelEthanolHCID 702—
Produkt4-(5-Chloro-2-methoxyphenyl)pyridazineHCID 5804226758%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

To an argon purged flask containing toluene (187 mL), ethanol (20.6 mL) and a 2M aqueous solution of sodium carbonate (132.3 mL) was added 4-bromopyridazine hydrobromide (Preparation 5, 15 g, 64 mmol), 5-chloro-2-methoxybenzeneboronic acid (13.4 g, 72 mmol) and tetrakis(triphenylphosphine) palladium (0) (3.2 g, 2.8 mmol). The flask was purged with argon again, then the reaction mixture heated to 110° C. for 4 hours. The mixture was filtered through Celite™ and the filtrate concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The organic layer was washed with water and brine, then dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude residue was dissolved in ethyl acetate and extracted with a 2M aqueous solution of hydrogen chloride (×3). The aqueous layer was basified with sodium hydrogen carbonate and extracted with ethyl acetate. The organic layer was then washed with water and brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to afford the title compound (8 g, 58%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08772293B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-b5fd5bf0c9cb498c85a9ce89b94337ca
Quellennotizuspto-grants-2014_07