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HRID 1916883作成日:2026年10月23日

4-Bromoaniline → HCID 178449870、化合物

https://huagongshe.com/ja/reaction/1916883

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromoanilineHCID 7807—
反応物2-(2-Fluorophenyl)-2-methylpropanenitrileHCID 11976441—
反応物TrimethylaluminumHCID 16682925—
溶媒TolueneHCID 1140—
生成物HCID 178449870HCID 17844987039%

反応条件

温度0 °C

反応手順

To an oven dried, N2 purged 250 mL round bottom flask attached with addition funnel was added 4-bromoaniline (7.31 g, 42.5 mmol) and anhydrous toluene (40 mL). To the reaction solution at 0° C. was added a 2.0 M Me3Al (32 mL, 1.5 molar equiv) solution. The reaction solution was stirred at 0° C. for 30 min, then a solution of 2-(2-fluorophenyl)-2-methylpropanenitrile (7.62 g, 46.7 mmol) in toluene (25 mL) was added to the reaction flask. The reaction solution was allowed to stir at 90° C. for 5 hr. The cooled reaction solution was quenched with an aq sodium potassium tartrate solution. After standing 20 min, the organic phase was partitioned and washed with sodium potassium tartrate solution. The organic solution was extracted with 1N aq HCl (100 mL×3). The combined aq HCl solution was neutralized by addition of 1N aq NaOH and extracted with dichloromethane (200 mL×2). The dichloromethane product solution was dried over Na2SO4, filtered, and concentrated in vacuo to afford the title compound (5.5 g, 39% yield). GCMS m/z=334, 336 [M]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08618154B2
出典データセットuspto-grants-2013_12
ORD IDord-ac6d2887a2ff4b399e550849d961e619
出典メモuspto-grants-2013_12