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HRID 502083作成日:2026年10月26日

Boron trifluoride etherate → 4-Bromo-1-chloro-2-(4-methoxybenzyl)benzene

https://huagongshe.com/reaction/502083

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluoride etherateHCID 8000—
反応物TriethylsilaneHCID 12052—
反応物Potassium HydroxideHCID 14797—
反応物(5-Bromo-2-chloro-phenyl)-(4-ethoxy-phenyl)-methanoneHCID 22328608—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物4-Bromo-1-chloro-2-(4-methoxybenzyl)benzeneHCID 22328594—

反応条件

温度47.5 °C

反応手順

A solution of 86.2 g (5-bromo-2-chloro-phenyl)-(4-methoxy-phenyl)-methanone and 101.5 ml triethylsilane in 75 ml dichloromethane and 150 ml acetonitrile is cooled to 10° C. Then with stirring 50.8 ml of boron trifluoride etherate are added so that the temperature does not exceed 20° C. The solution is stirred for 14 h at ambient temperature, before another 9 ml triethylsilane and 4.4 ml boron trifluoride etherate are added. The solution is stirred for a further 3 h at 45-50° C. and then cooled to ambient temperature. A solution of 28 g potassium hydroxide in 70 ml of water is added and the mixture is stirred for 2 h. Then the organic phase is separated off and the aqueous phase is extracted another three times with diisopropylether. The combined organic phases are washed twice with 2 M potassium hydroxide solution and once with aqueous sodium chloride solution and then dried over sodium sulfate. After the solvent is removed the residue is washed with ethanol and dried at 60° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772378B2
出典データセットuspto-grants-2010_08
ORD IDord-2f6c5387dd2744af8518c21aa8765869
出典メモuspto-grants-2010_08