HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665587Generated: October 29, 2026
HCID 17683255, compound → 1-[2-(Trifluoromethyl)benzoyl]piperazine
https://huagongshe.com/reaction/1665587
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 17683255 | HCID 17683255 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[2-(Trifluoromethyl)benzoyl]piperazine | HCID 16733784 | 86.2% |
Reaction Steps
NH4COOH (15.5 g, 247 mmol) and 10% Pd/C (1.8 g) in water (2 mL) were added to a stirred solution of (4-benzyl-piperazin-1-yl)-(2-trifluoromethyl-phenyl)-methanone (8.6 g, 24.7 mmol) in MeOH (40 mL) and the resulting mixture was heated to reflux at 75° C. for 4 hrs. The reaction mixture was then filtered over celite and the filtrate evaporated. The resulting residue was dissolved in ethyl acetate, washed with 10% NaOH solution then brine solution, dried over Na2SO4 and concentrated under reduced pressure to afford 5.5 g (86%) of piperazin-1-yl-(2-trifluoromethyl-phenyl)-methanone. 1H NMR: (DMSO-d6): δ 7.8 (d, 1H), 7.7 (t, 1H), 7.6 (t, 1H), 7.4 (d, 1H), 3.5 (m, 2H), 3.0 (m, 2H), 2.7 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039463B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-25683c178b354bc98ffc34429179486d |
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| Source note | uspto-grants-2011_10 |
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