참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Bromopropane | HCID 6358 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3,4,5-Trimethoxyphenylacetonitrile | HCID 25887 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-Methyl-2-(3,4,5-trimethoxyphenyl)butanenitrile | HCID 4661574 | 54.2% |
반응 단계
With stirring under ice cooling, 20.25 g (97.7 mmols) of 3,4,5-trimethoxyphenylacetonitrile was added by small portions to 50 ml of a solution of 2.45 g (102.1 mmols) of sodium hydride in dimethylformamide. The solution was dropwise added to 100 ml of a solution of 12.45 g (101.2 mmols) of 2-bromopropane in dimethylformamide with stirring under ice cooling. The mixture was stirred under ice cooling for further 3 hours. After the reaction, an aqueous saturated sodium bicarbonate solution was added to the mixture followed by extraction of the solution with ethyl acetate. The ethyl acetate layer was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate =4/1) to afford 13.2 g (yield: 54%) of 3-methyl-2-(3,4,5-trimethoxyphenyl)butyronitrile.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05053408 |
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| 출처 데이터셋 | uspto-grants-1991_10 |
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| ORD ID | ord-2e80f1fe8b8e49ef8601f4714a0385df |
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| 출처 메모 | uspto-grants-1991_10 |
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