참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Fluoro-3-nitrobenzoic acid | HCID 67987 | — |
| 반응물 | Bis(2,2,2-trifluoroethyl)amine | HCID 78999 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | DCM thionyl chloride | HCID 21879677 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-Fluoro-3-nitro-N,N-bis(2,2,2-trifluoroethyl)benzamide | HCID 58911744 | — |
반응 단계
4-Fluoro-3-nitrobenzoic acid (2.50 g, 13.5 mmol) was refluxed in a 2:1 mixture of CH2Cl2/SOCl2 (150 mL) for 5 h. The solvent was concentrated and the residue was dissolved in CH2Cl2 (50 mL). Another CH2Cl2 solution (50 mL) of diisopropylethylamine (DIPEA) (3.50 mL, 20.3 mmol) and bis(2,2,2-trifluoroethyl)amine (4.90 g, 27.0 mmol) was then added dropwise to the cold stirring solution (0° C.) of the acid chloride. The solution was stirred at rt overnight. The solution was then washed with 5% KHSO4 solution, saturated NaHCO3 solution, brine and dried over anhydrous MgSO4. The crude product was purified by flash chromatography using 3:1/hexanes:EtOAc to afford the title product. Yield: 3.08 g (66%). 1H NMR (400 MHz, CDCl3) δ 4.17 (brs, 4H), 7.40 (t, J=8.59 Hz, 1H), 7.66 (m, 2H), 8.10 (d, J=6.84 Hz, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07244850B2 |
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| 출처 데이터셋 | uspto-grants-2007_07 |
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| ORD ID | ord-7ef732435ffc410794416f0089413b14 |
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| 출처 메모 | uspto-grants-2007_07 |
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