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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042716Generated: November 1, 2026

Ethylenediamine → 1-[2-Amino-4-(trifluoromethyl)phenyl]pyrrolidin-2-one

https://huagongshe.com/reaction/1042716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantPotassium CarbonateHCID 11430—
Reactant2-PyrrolidoneHCID 12025—
Reactant2-Bromo-5-(trifluoromethyl)benzenamineHCID 67989—
CatalystCopper iodideHCID 83717—
SolventTolueneHCID 1140—
Product1-[2-Amino-4-(trifluoromethyl)phenyl]pyrrolidin-2-oneHCID 16786761—

Reaction Conditions

Temperature80 °C

Reaction Steps

A resealable tube was charged with 2-bromo-5-(trifluoromethyl)aniline (1.00 g, 4.16 mmol), 2-pyrrolidinone (0.425 g, 5.00 mmol), N,N′-ethylene diamine (0.037 g, 0.42 mmol), potassium carbonate (1.15 g, 8.32 mmol), copper iodide (0.80 mg, 0.42 mmol) and toluene (1.0 mL). The tube was sealed and the mixture was heated at 80° C. for 24 h. The resulting mixture was partitioned between ethyl acetate and water. The organic phase was separated, dried over anhydrous sodium sulfate, filtered, and concentrated. The residue was purified via column chromatography on silica gel (gradient elution with 0-100% ethyl acetate-hexane) to afford 1-(2-amino-4-(trifluoromethyl)phenyl)pyrrolidin-2-one as a gray solid. MS m/z=245 [M+H]+. Calc'd for C11H11F3N2O: 244.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557996B2
Source datasetuspto-grants-2013_10
ORD IDord-e45abc9924cb46b0a8cc809dc1c5e00e
Source noteuspto-grants-2013_10