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HRID 17903作成日:2026年10月26日

1-Bromo-2-Chloroethane → 1-(2,2-Difluorobenzo[D][1,3]dioxol-5-YL)cyclopropanecarbonitrile

https://huagongshe.com/reaction/17903

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2,2-Difluoro-1,3-benzodioxole-5-acetonitrileHCID 20311384—
触媒Benzyl triethylammonium chlorideHCID 66133—
溶媒WaterHCID 962—
生成物1-(2,2-Difluorobenzo[D][1,3]dioxol-5-YL)cyclopropanecarbonitrileHCID 57446150—

反応条件

温度70 °C

反応手順

Sodium hydroxide (50% aqueous solution, 10 mL) was slowly added to a mixture of crude (2,2-difluoro-benzo[1,3]dioxol-5-yl)-acetonitrile, benzyltriethylammonium chloride (3.00 g, 15.3 mmol), and 1-bromo-2-chloroethane (4.9 g, 38 mmol) at 70° C. The mixture was stirred overnight at 70° C. before the reaction mixture was diluted with water (30 mL) and extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and evaporated to dryness to give crude 1-(2,2-difluoro-benzo[1,3]dioxol-5-yl)-cyclopropanecarbonitrile, which was used directly in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741321B2
出典データセットuspto-grants-2010_06
ORD IDord-e843f72fe235471d8175384cfbb0c682
出典メモuspto-grants-2010_06