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HRID 458278作成日:2026年10月26日

Hexane → 3,5-Dichloro-4-trimethylsilyl-bromobenzene

https://huagongshe.com/reaction/458278

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物Trimethylsilyl triflateHCID 65367—
反応物5-Bromo-1,3-dichloro-2-iodobenzeneHCID 4574491—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
生成物3,5-Dichloro-4-trimethylsilyl-bromobenzeneHCID 2307169190%

反応手順

The 2,6-Dichloro-4-bromoiodobenzene (4.48 g, 12.7 mmol) was dissolved in diethyl ether (50 ml). To the solution was then added dropwise a hexane solution of n-butyl lithium (1.56 M, 8.2 ml) at −78° C. At the same temperature, the mixture was then stirred for 1 hour. To the mixture was then added dropwise trimethylsilyl trifluoromethanesulfonate (3.2 ml, 16.5 mmol). The mixture was then stirred at −78° C. for 1 hour and at room temperature for 30 minutes. After the quenching of the reaction with water, the mixture was then extracted with ether. The resulting organic phase was then dried over magnesium sulfate. The solvent was then distilled off. The crude product thus obtained was then distilled under reduced pressure in a glass tube oven so that it was purified to obtain 3,5-dichloro-4-trimethylsilyl-bromobenzene (3.39 g; yield: 90%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07189790B2
出典データセットuspto-grants-2007_03
ORD IDord-659b6c0f088d4756b4a3d2c014389226
出典メモuspto-grants-2007_03