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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2044201Generated: October 31, 2026

Potassium Carbonate → 5-ethyl-2-(2'-fluoro-4'-methyl-3'-trifluoromethylanilino)phenylacetic acid N,N-dimethyl amide

https://huagongshe.com/reaction/2044201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-dimethyl-5-ethyl-2-iodophenylacetamideHCID 21938643—
Reactant2-fluoro-N-methyl-3-(trifluoromethyl)anilineHCID 68821735—
CatalystCopperHCID 23978—
SolventEthyl AcetateHCID 8857—
Product5-ethyl-2-(2'-fluoro-4'-methyl-3'-trifluoromethylanilino)phenylacetic acid N,N-dimethyl amideHCID 68998379—

Reaction Steps

A mixture of N,N-dimethyl-5-ethyl-2-iodophenylacetamide (2.0 g, 6.3 mmol), 2-fluoro-methyl-3-trifluoromethylaniline (2.4 g, 12.6 mmol), copper (0.2 g, 3.2 mmol), cuprous iodide (0.6 g, 3.2 mmol), and K2CO3 (0.9 g, 6.3 mmol) in xylenes (6.0 mL) are heated at reflux for 24 h. After cooling, the crude reaction mixture is diluted with EtOAc and filtered through Celite®. The filtrate is concentrated under reduced pressure. The residue is purified by flash chromatography, eluting with hexanes, then up to 25% EtOAc/hexane mixtures to give the target compound 5-ethyl-2-(2′-fluoro-4′-methyl-3′-trifluoromethylanilino)phenylacetic acid N,N-dimethyl amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586782B2
Source datasetuspto-grants-2013_11
ORD IDord-b988099f036c4bb8993d28c8e4a56da5
Source noteuspto-grants-2013_11