HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550814Generated: October 26, 2026
Pyridine → 1-Piperazinecarbonyl chloride, 4-[3-(trifluoromethyl)phenyl]-
https://huagongshe.com/reaction/550814
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-(3-(Trifluoromethyl)phenyl)piperazine | HCID 4296 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Piperazinecarbonyl chloride, 4-[3-(trifluoromethyl)phenyl]- | HCID 59011936 | 79% |
Reaction Steps
A mixture of triphosgene (3.2 g, 10.85 mmol) in tetrahydrofuran (10 mL) was slowly treated with pyridine (1.72 g, 21.72 mmol) via syringe. The resulting white suspension was then treated portionwise with 1-[3-(trifluoromethyl)phenyl]piperazine (500 mg, 2.17 mmol). The reaction mixture was allowed to stir at 25° C. for 18 h. At this time, the reaction was slowly quenched by the addition of water. The aqueous layer was extracted with methylene chloride. The organics were washed with a saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered and concentrated in vacuo to afford 4-(3-trifluoromethyl-phenyl)piperazine-1-carbonyl chloride (500 mg, 79%). The NMR spectrum obtained on the sample is compatible with its structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07947692B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-2fcd49d7186a4f688005b1d98888c598 |
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| Source note | uspto-grants-2011_05 |
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