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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Piperazin-2-one | HCID 231360 | — |
| Reactant | 4-methyl-2-(trifluoromethyl)benzoyl Chloride | HCID 2775606 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-{[4-Methyl-2-(trifluoromethyl)phenyl]carbonyl}-2-piperazinone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501946B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-e4247b1912ab4cfd9df086607d116809 |
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| Source note | uspto-grants-2013_08 |
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