HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327206Generated: October 26, 2026
1,1'-Carbonyldiimidazole → N-[4-(3-Fluorophenylcarbonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropanamide
https://huagongshe.com/reaction/327206
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 3,3,3-Trifluoro-2-hydroxy-2-(trifluoromethyl)propionic Acid | HCID 2725043 | — |
| Reactant | 4-Amino-3'-fluorobenzophenone | HCID 10798712 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[4-(3-Fluorophenylcarbonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropanamide | HCID 21480107 | 55.2% |
Reaction Steps
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, 2H, aromatic) 7.94-7.98 (m, 2H, aromatic) 9.84 (s, 1H, NH) 10.85 (bs, 1H, OH). MS (CI, CH4): 410 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05272163 |
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| Source dataset | uspto-grants-1993_12 |
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| ORD ID | ord-828cfaa48ce34f49a91b536d02abe3e4 |
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| Source note | uspto-grants-1993_12 |
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