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HRID 1619625作成日:2026年10月27日

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

https://huagongshe.com/reaction/1619625

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Sodium CarbonateHCID 10340—
反応物5-Chloro-2-methoxyphenylboronic acidHCID 2735751—
反応物4-Bromopyridazine hydrobromideHCID 53407906—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒EthanolHCID 702—
生成物4-(5-Chloro-2-methoxyphenyl)pyridazineHCID 5804226758%

反応条件

温度110 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08772293B2
出典データセットuspto-grants-2014_07
ORD IDord-b5fd5bf0c9cb498c85a9ce89b94337ca
出典メモuspto-grants-2014_07