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HRID 1619626作成日:2026年10月25日

Boron tribromide → 4-Chloro-2-pyridazin-4-ylphenol

https://huagongshe.com/reaction/1619626

反応式

関与物質

役割名称HCID仕込み量
反応物Boron tribromideHCID 25134—
反応物4-(5-Chloro-2-methoxyphenyl)pyridazineHCID 58042267—
溶媒DichloromethaneHCID 6344—
生成物4-Chloro-2-pyridazin-4-ylphenolHCID 13620087580%

反応手順

To a stirred solution of 4-(5-chloro-2-methoxyphenyl)pyridazine (Preparation 6, 22 g, 100 mmol) in dichloromethane (200 mL) at 0° C. was added drop wise a solution of boron tribromide (48 mL, 499 mmol) in dichloromethane (200 mL). The reaction mixture was stirred at room temperature for 18 hours. The reaction was quenched by pouring onto crushed ice and basifying the mixture to pH 8 with sodium hydrogen carbonate. The mixture was extracted with dichloromethane. The aqueous layer was extracted further with ethyl acetate. The organics were combined and dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude residue was purified by silica gel column chromatography (0%-4% methanol in dichloromethane gradient elution) to afford the title compound (16.5 g, 80%)

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-77d15c7698254faa8122f140fbe9e113
出典メモuspto-grants-2014_07