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HRID 358378作成日:2026年10月25日

Benzene → N-Methyl-N-(tert-butyldimethylsilyl)trifluoroacetamide

https://huagongshe.com/reaction/358378

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物Sodium hydrideHCID 24758—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物Acetamide, 2,2,2-trifluoro-N-methyl-HCID 69948—
溶媒AcetonitrileHCID 6342—
生成物N-Methyl-N-(tert-butyldimethylsilyl)trifluoroacetamideHCID 2724275—

反応手順

To 800 ml of dry benzene:acetonitrile (v/v, 1:1) was added 127 g (1.0 mole) of N-methyl-trifluoroacetamide. To this solution, while stirring and maintaining the temperature at 0 degress C., was slowly added 23.5 g (0.98 mole) of sodium hydride. The solution was then stirred for 4 hours at 4 degrees C. At this time, 173.34 g (1.15 mole) of t-butyldimethylsilyl chloride was added in four equal aliquots over a period of 80 minutes. After the last addition the solution was stirred for 2 hours at 4 degrees C. The precipitate of sodium chloride was then removed from the reaction mixture by filtration under dry nitrogen and the resulting filter cake washed twice with 100 ml each of dry benzene. Washings and filtrate were combined and concentrated. The remaining yellow solution was fractionally distilled with the distillate at 158-172 degrees C. being collected. Redistillation of this fraction gave the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04467037
出典データセットuspto-grants-1984_08
ORD IDord-42fe8ff05edf4687a2f49e3dbd7652d5
出典メモuspto-grants-1984_08