戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 500147作成日:2026年10月25日

1-Bromo-2-Chloroethane → 1-(Quinolin-6-yl)cyclopropanecarbonitrile

https://huagongshe.com/reaction/500147

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-2-ChloroethaneHCID 7849—
反応物Sodium HydroxideHCID 14798—
反応物(Quinolin-6-yl)acetonitrileHCID 21992552—
触媒Benzyl triethylammonium chlorideHCID 66133—
溶媒WaterHCID 962—
生成物1-(Quinolin-6-yl)cyclopropanecarbonitrileHCID 66812840—

反応条件

温度50 °C

反応手順

60 mL of 50% aqueous sodium hydroxide was added to a mixture of 1-bromo-2-chloroethane (22.0 mL, 265 mmol), quinolin-6-ylacetonitrile (16.0 g, 66.6 mmol), and benzyltriethylammonium chloride (990 mg, 4.3 mmol) at 50° C. The reaction mixture was stirred at 50° C. for 3 h. After cooling to RT, the reaction mixture was poured into 100 mL water, and extracted with dichloromethane (3×100 mL). The combined organic extracts were dried over sodium sulfate, filtered through a pad of silica gel eluting with 20% ethyl acetate in dichloromethane. The filtrate was concentrated to give the desired product which was used in the next step without further purification. (12.4 g, 96%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07767675B2
出典データセットuspto-grants-2010_08
ORD IDord-ed80d26b07bf4ccabaf75272fc1f10e9
出典メモuspto-grants-2010_08