HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820624Generated: November 2, 2026
2-(Trifluoromethyl)benzoyl chloride → HCID 66906079, compound
https://huagongshe.com/reaction/1820624
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Trifluoromethyl)benzoyl chloride | HCID 67561 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(5-Nitropyridin-2-yl)piperazine | HCID 2928799 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66906079 | HCID 66906079 | 41% |
Reaction Steps
2-(Trifluoromethyl)benzoyl chloride (2.0 mL, 11.0 mmol) was added slowly to a solution of 1-(5-nitropyridin-2-yl)piperazine (2.0 g, 10 mmol) and diisopropylethylamine (3.5 mL, 20 mmol) in Dichloromethane (15 mL) at 0° C. under argon. The mixture was then stirred at 25° C. for 2 h. The reaction was quenched with H2O. The aqueous phase was extracted with ethyl acetate. The organic phase was washed with saturated NaCl and dried over anhydrous MgSO4. The organic phase was concentrated and then purified by column chromatography to yield [4-(5-nitropyridin-2-yl)piperazin-1-yl]-(2-trifluoromethylphenyl)methanone as a yellow solid (1.55 g, 41% yield). MS (ES+) m/z 381.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605161B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-06c40a600d0f4c52b4b3e7e73f64a2ee |
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| Source note | uspto-grants-2009_10 |
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