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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889014Generated: October 29, 2026

Triethylamine → 4-{[4-Methyl-2-(trifluoromethyl)phenyl]carbonyl}-2-piperazinone

https://huagongshe.com/reaction/1889014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPiperazin-2-oneHCID 231360—
Reactant4-methyl-2-(trifluoromethyl)benzoyl ChlorideHCID 2775606—
SolventDichloromethaneHCID 6344—
Product4-{[4-Methyl-2-(trifluoromethyl)phenyl]carbonyl}-2-piperazinoneHCID 66599410—

Reaction Steps

2-piperazinone (0.400 g, 4 mmol, commercially available from e.g. Sigma-Aldrich) was dissolved in dichloromethane (DCM) (20 mL), and to this was added triethylamine (0.669 mL, 4.80 mmol). The solution was then cooled to 0° C. before 4-methyl-2-(trifluoromethyl)benzoyl chloride (I62) (0.979 g, 4.40 mmol) in dichloromethane (DCM) (5 mL) was added dropwise. The solution was stirred, under argon, for 30 minutes before the solvent was evaporated in vacuo. The remaining residue was then re-dissolved in DCM (40 mL) and washed with water (20 mL), a saturated solution of sodium bicarbonate (20 mL) and brine (20 mL), before being dried over anhydrous sodium sulphate. The sodium sulphate was then removed by filtration and the solvent was evaporated in vacuo. The remaining solid was then stirred in hexane (40 mL) at 55° C. for 30 minutes. The solid was then removed by filtration to yield the product in 1.110 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501946B2
Source datasetuspto-grants-2013_08
ORD IDord-e4247b1912ab4cfd9df086607d116809
Source noteuspto-grants-2013_08