참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Chloro-4-(trifluoromethyl)phenol | HCID 2736603 | — |
| 반응물 | N,N-diethyl-5-fluoro-2-nitrobenzamide | HCID 12999068 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Benzene hexane | HCID 110624 | — |
| 생성물 | 5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide | HCID 15335019 | 81.6% |
반응 단계
To a 100 ml flask fitted with a magnetic stirrer and drying tube is added dimethyl sulfoxide (30 ml), anhydrous potassium carbonate (7.55 g, 0.054 mole) and 2-chloro-4-trifluoromethylphenol (10.3 g, 0.052 mole). The mixture is stirred at room temperature overnight. A solution of N,N-diethyl-5-fluoro-2-nitrobenzamide (12.5 g, 0.052 mole) in dimethyl sulfoxide (20 ml) is then added rapidly and the reaction mixture is stirred at room temperature for 60 hours. The reaction mixture is poured into water (500 ml) and the product extracted into carbon tetrachloride (4×100 ml), the combined extracts are dried over anhydrous magnesium sulfate and the solvent removed under vacuum to afford 15.3 g of 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzamide (75% yield) Recrystallization from benzene/hexane affords substantially pure product mp. 75°-79° C. Elemental anal, Calcd. for C18H16ClF3N2O4 : C, 51.80; H, 3.88; Cl, 8.55; F, 13.68; N, 6.73. Found: C, 52.03; H, 3.90; Cl, 8.54; F, 13.59; N, 6.83.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04259510 |
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| 출처 데이터셋 | uspto-grants-1981_03 |
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| ORD ID | ord-58e228bb23604395be2422d3b310d73b |
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| 출처 메모 | uspto-grants-1981_03 |
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