Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2259698생성일: 2026년 10월 26일
1,1'-Carbonyldiimidazole → N-[4-(3-Fluorophenylcarbonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropanamide
https://huagongshe.com/reaction/2259698
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | 3,3,3-Trifluoro-2-hydroxy-2-(trifluoromethyl)propionic Acid | HCID 2725043 | — |
| 반응물 | 4-Amino-3'-fluorobenzophenone | HCID 10798712 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-[4-(3-Fluorophenylcarbonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropanamide | HCID 21480107 | 55.2% |
반응 단계
To a stirred solution of 3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropanoic acid (1.17 g, 5.5 mmol) in dry tetrahydrofuran (35 mL) was added 1,1'-carbonyldiimidazole (0.89 g, 5.5 mmol). The mixture was heated at reflux for 45 minutes, then cooled to room temperature. 4-Amino-3'-fluorobenzophenone (1.08 g, 5.0 mmol) was added in one portion and the reaction mixture heated at reflux for 48 hours. Tetrahydrofuran was removed from the reaction mixture in vacuo, and the residue dissolved in ethyl ether and filtered. The filtrate was washed with 3N HCl (50 mL) and water. The ether extract was dried (MgSO4) and concentrated in vacuo to an off-white solid. Purification by flash column chromatography (5% v/v ethyl ether/methylene chloride) yielded the title propanamide as a tan solid (1.13 g, 55%); mp 169°-171° C. 1H-NMR (300 MHz, d6 -DMSO): 7.50-7.64 (m, 4H, aromatic) 7.77-7.82 (m, 2 H, aromatic) 7.94-7.98 (m, 2H, aromatic) 9.84 (s, 1H, NH) 10.85 (bs, 1H, OH). MS (CI, CH4): 410 (M+1). Analysis for C17H10F7NO3 : Calculated: C, 49.89; H, 2.46; N, 3.42. Found: C, 49.60; H, 2.43; N, 3.34.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05474999 |
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| 출처 데이터셋 | uspto-grants-1995_12 |
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| ORD ID | ord-1a3a93147c454738a47fe8d8dd9c8047 |
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| 출처 메모 | uspto-grants-1995_12 |
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