참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol, 1-ethoxy-2,2,2-trifluoro- | HCID 9897 | — |
| 반응물 | 4-Chlorobenzamide | HCID 12084 | — |
| 반응물 | Sodium Sulfate | HCID 24436 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 4-chloro-N-(2,2,2-trifluoro-1-hydroxyethyl)benzamide | HCID 11322758 | — |
반응 단계
A solution of 4-chlorobenzamide (22.0 g, 0.141 mol) and trifluoroacetaldehyde ethyl hemiacetal (25.0 g as is, 22.5 g real, 0.156 mol) in dioxane (200 mL) is treated with anhydrous sodium sulfate (10 g, to dry the 10% water in the hemiacetal) and refluxed for 60 hours. The solids are filtered and the filtrate is evaporated to a solid. The solids are dissolved in about 200 mL of 15% ethyl acetate in heptane. Unreacted starting material (5.6 g) crystallizes out and is filtered. The title product is obtained from the mother liquors as a white crystalline solid (22.1 g, 82.9% based on recovery of starting material): mp 139.5-140.5° C.; characterized by 1H and 19F NMR and Mass spectra. 1H NMR (DMSO-d6) δ9.45 (d, J=8.7 Hz, NH), 7.93, 7.54 (AB with fine splitting, J=8.4 Hz, ArH), 7.54 (broad s, OH), 5.90 (m, J=8.7, 2.9, 5.8 Hz, CH); 19F NMR δ−80.3 (d, J=5 Hz).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06596902B2 |
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| 출처 데이터셋 | uspto-grants-2003_07 |
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| ORD ID | ord-f28b91eb54054a85913918398751affb |
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| 출처 메모 | uspto-grants-2003_07 |
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