HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502760Generated: October 26, 2026
Ethylenediamine → 1-[2-Amino-4-(trifluoromethyl)phenyl]pyrrolidin-2-one
https://huagongshe.com/reaction/502760
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Pyrrolidone | HCID 12025 | — |
| Reactant | 2-Bromo-5-(trifluoromethyl)benzenamine | HCID 67989 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-[2-Amino-4-(trifluoromethyl)phenyl]pyrrolidin-2-one | HCID 16786761 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776869B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-2cd0d031b196476493fe1db15da15114 |
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| Source note | uspto-grants-2010_08 |
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