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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

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물3,3,3-Trifluoro-2-hydroxy-2-(trifluoromethyl)propionic AcidHCID 2725043—
반응물4-Amino-3'-fluorobenzophenoneHCID 10798712—
용매TetrahydrofuranHCID 8028—
생성물N-[4-(3-Fluorophenylcarbonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropanamideHCID 2148010755.2%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05474999
출처 데이터셋uspto-grants-1995_12
ORD IDord-1a3a93147c454738a47fe8d8dd9c8047
출처 메모uspto-grants-1995_12