참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Cyclohexylethanol | HCID 20508 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-Fluoro-2-(trifluoromethyl)benzaldehyde | HCID 522940 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | HCID 86658987 | HCID 86658987 | 75.6% |
반응 단계
Sodium hydride (343.2 mg, 8.58 mmol, 60% dispersed oil) was slowly added to cyclohexaneethanol (1 g, 7.8 mmol) dissolved in 30 ml of dried dimethylformamide under nitrogen at room temperature while stirring. The mixture was further stirred at room temperature for 30 minutes. Then, 4-fluoro-2-(trifluoromethyl)benzaldehyde (1.2 g, 7.8 mmol) dissolved in dried dimethylformamide was added thereto over 10 minutes and stirred at room temperature for 18 hours until the initial product disappeared. Subsequently, ice water was added thereto, and the resulting mixture was extracted with ethyl acetate and water. The organic layer was washed with water several times, dried with anhydrous magnesium sulfate, filtered and solvent-evaporated. The residual oil was chromatographed on the silica gel column (hexane:ethyl acetate-20:1) to afford the intermediate, 4-(2-cyclohexylethoxy)-2-(trifluoromethyl)benzaldehyde (1.77 g, yield: 75.6%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08637558B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-9c081e498bc144e4aa60dc4f5d0a06c4 |
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| 출처 메모 | uspto-grants-2014_01 |
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