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HRID 982978作成日:2026年10月25日

p-Bromochlorobenzene → 4-(4-Chloro-phenyl)-1H-indole

https://huagongshe.com/reaction/982978

反応式

関与物質

役割名称HCID仕込み量
反応物p-BromochlorobenzeneHCID 7806—
反応物Sodium HydroxideHCID 14798—
反応物1H-Indole-4-boronic acid, pinacol esterHCID 11322471—
触媒PalladiumHCID 23938—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物4-(4-Chloro-phenyl)-1H-indoleHCID 2256174789%

反応条件

温度70 °C

反応手順

To a mixture of 4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-indole (3, 2.43 g, 10 mmol), and 4-bromochlorobenzene (2.87 g, 15 mmol) in THF (34 mL)) were added Palladium catalyst Pd(PPh3)4 (347 mg, 0.3 mmol) and the freshly prepared sodium hydroxide solution (1.20 g, 30 mmol in 14 mL water). The system was degassed and then charged with nitrogen. The degas procedure was repeated for three times. The mixture was stirred under nitrogen at 70° C. oil bath for 15 hours. TLC showed the completion of the coupling reaction. The mixture was cooled to room temperature, diluted with ethyl acetate, and separated from water layer. The ethyl acetate solution was washed by brine, dried over Na2SO4, and concentrated. The crude product was purified by a silica gel column eluting with hexanes-EtOAc (9:1) to provide 2.02 g (89%) of the product 4-(4-chloro-phenyl)-1H-indole as a white 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-9bd719bd920742fe9ad0cf4bd000bd15
出典メモuspto-grants-2005_03