HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550853Generated: October 25, 2026
Pyridine → 4-(3-Trifluoromethyl-benzyl)-piperazine-1-carbonyl chloride
https://huagongshe.com/reaction/550853
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triphosgene | HCID 94429 | — |
| Reactant | 1-(3-(Trifluoromethyl)benzyl)piperazine | HCID 2060855 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(3-Trifluoromethyl-benzyl)-piperazine-1-carbonyl chloride | HCID 59011960 | 92.8% |
Reaction Steps
A magnetically stirred mixture of triphosgene (365 mg, 1.23 mmol) in tetrahydrofuran (20 mL) under a nitrogen atmosphere was treated slowly with pyridine (485 mg, 6.15 mmol) via syringe. The resulting white suspension was then treated with a solution of 1-(3-Trifluoromethyl-benzyl) piperazine (1.0 g, 4.10 mmol) in tetrahydrofuran (10 mL) via addition funnel over 10 min. The reaction mixture was stirred at 25° C. overnight. At this time, the reaction was filtered to remove solids. The filtrate was then concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 60:40 hexanes/ethyl acetate afforded 4-(3-Trifluoromethyl-benzyl)-piperazine-1-carbonyl chloride (350 mg, 28%) as a clear oil. 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-c3155bcea5e3487984b9722812f8915f |
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| Source note | uspto-grants-2011_05 |
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