戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1157420作成日:2026年10月25日

Boron tribromide → 3-Chloro-5-(2-chloro-3-fluoro-5-hydroxyphenoxy)benzonitrile

https://huagongshe.com/reaction/1157420

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3-Chloro-5-(2-chloro-3-fluoro-5-methoxyphenoxy)benzonitrileHCID 44549247—
溶媒DichloromethaneHCID 6344—
生成物3-Chloro-5-(2-chloro-3-fluoro-5-hydroxyphenoxy)benzonitrileHCID 4455096935%

反応条件

温度0 °C

反応手順

Under nitrogen atmosphere, 3-chloro-5-(2-chloro-3-fluoro-5-methoxyphenoxy)-benzonitrile (50-4) (9.6 g, 30.8 mmol) was diluted in CH2Cl2 (60 mL, 0.5M) and then cooled to 0° C. To this solution BBr3 (61.5 mL, 61.5 mmol, 1M in CH2Cl2) was slowly added to the reaction. The reaction mixture was allowed to slowly warm to room temperature and stir for 12 hours. It was then cooled to 0° C. and slowly quenched with water (60 mL). The aqueous layer was then extracted with methylene chloride (3×30 mL). The organic extracts were dried over sodium sulfate and concentrated. Silica gel chromatography (1%-20% EtOAc/Hexanes) gave 3-chloro-5-(2-chloro-3-fluoro-5-hydroxyphenoxy)benzonitrile (50-5) (3.2 g, 35%). LCMS (ES) m/z 298.2 (M)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07807684B2
出典データセットuspto-grants-2010_10
ORD IDord-525a9a5d52b949f5bab1baf7ee3f0231
出典メモuspto-grants-2010_10