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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 17683255HCID 17683255—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1-[2-(Trifluoromethyl)benzoyl]piperazineHCID 1673378486.2%

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039463B2
Source datasetuspto-grants-2011_10
ORD IDord-25683c178b354bc98ffc34429179486d
Source noteuspto-grants-2011_10