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HRID 3903作成日:2026年10月24日

Chlorotrimethylsilane → 2,2-Bis(4-trimethylsilylphenyl)hexafluoropropane

https://huagongshe.com/ja/reaction/3903

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物2,2-Bis(4-bromophenyl)hexafluoropropaneHCID 13878551—
反応物Acetone cardiceHCID 18522661—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物2,2-Bis(4-trimethylsilylphenyl)hexafluoropropaneHCID 13878552—

反応条件

温度-78 °C

反応手順

To a solution of 4.62 g (0.1 mole) 2,2-bis(4-bromophenyl)hexafluoropropane in 75 ml of anhydrous tetrahydrofuran was added dropwise 28 ml (0.4 moles) of a 1.4 molar solution of n-butyllithium in hexane while the reaction mixture was cooled in a dry ice-acetone slush. The reaction mixture was stirred for one half hour at -78° C. A dropwise addition of chlorotrimethylsilane (5 ml, 0.04 moles) was then made to the reaction mixture at -78° C. The stirring slurry was allowed to come to ambient temperature over 16 hours. To the reaction mixture was added 100 ml hexane. The organic layer was washed with 2×150 ml saturated sodium chloride solution and 2×150 ml water. The organic layer was dried, filtered, and concentrated to yield the white crystalline product 2,2-bis(4-trimethylsilylphenyl)hexafluoropropane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04722985
出典データセットuspto-grants-1988_02
ORD IDord-c8ad3021517e47849a4ef0618fa4b5f1
出典メモuspto-grants-1988_02