참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzene | HCID 241 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 반응물 | Acetamide, 2,2,2-trifluoro-N-methyl- | HCID 69948 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | N-Methyl-N-(tert-butyldimethylsilyl)trifluoroacetamide | HCID 2724275 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04467037 |
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| 출처 데이터셋 | uspto-grants-1984_08 |
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| ORD ID | ord-42fe8ff05edf4687a2f49e3dbd7652d5 |
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| 출처 메모 | uspto-grants-1984_08 |
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