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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant3,3,3-Trifluoro-2-hydroxy-2-(trifluoromethyl)propionic AcidHCID 2725043—
Reactant4-Amino-3'-fluorobenzophenoneHCID 10798712—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-(3-Fluorophenylcarbonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-trifluoromethylpropanamideHCID 2148010755.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05272163
Source datasetuspto-grants-1993_12
ORD IDord-828cfaa48ce34f49a91b536d02abe3e4
Source noteuspto-grants-1993_12