戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 983010作成日:2026年10月26日

Acetic Acid → 4-(3-Bromo-phenyl)1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/983010

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物PyridiniumtribromideHCID 21124087—
反応物4-(3-Bromo-phenyl)-1H-indoleHCID 22561906—
触媒ZincHCID 23994—
溶媒t-BuOH ethanol aceticacidHCID 86587657—
生成物4-(3-Bromo-phenyl)1,3-dihydro-indol-2-oneHCID 2256184965%

反応条件

温度27 °C

反応手順

To the suspension of 4-(3-bromo-phenyl)-1H-indole (1.48 g, 5.44 mmol) in t-BuOH-ethanol-acetic acid (3:2:1) (66 mL) was added pyridinium tribromide (90% purity from Aldrich, 5.80 g, 16.3 mmol)) portionwise. The mixture was stirred at 27° C. for 3 hours, and then to the mixture was added acetic acid (26 mL). Zinc dust was added to the reaction mixture portionwise until the color changed from deep red to light yellow, and the reaction mixture was stirred at room temperature for one hour. The unreacted zinc dust was filtered off and washed with ethanol. The filtrate was concentrated, and the syrupy residue was dissolved in ethyl acetate, which was washed with water, 0.5 N HCl, sat. NaHCO3 and brine, and dried over Na2SO4. After filtration and evaporation, the crude product was triturated with diethyl ether to provide product 4-(3-bromo-phenyl)-1,3-dihydro-indol-2-one (1.02 g, 65%) as a tan solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06861418B2
出典データセットuspto-grants-2005_03
ORD IDord-fa5c429054d34c36a1b1d6e08887fb8e
出典メモuspto-grants-2005_03