HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727175Generated: November 2, 2026
Cyclopentanecarbonyl chloride → 1-Cyclopentanecarbonylpiperazine
https://huagongshe.com/reaction/1727175
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclopentanecarbonyl chloride | HCID 78284 | — |
| Reactant | Piperazine, hexahydrate | HCID 120181 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Cyclopentanecarbonylpiperazine | HCID 15512779 | — |
Reaction Steps
Piperazine hexahydrate (8.55 g, 44.0 mmol) was dissolved in absolute ethanol (50 ml) and then refluxed for 10 min. Cyclopentanecarbonyl chloride (5.83 g, 44 mmol) was added dropwise at 65° C. and the reaction mixture was refluxed for 30 min and then stirred at room temperature for 18 h. The reaction mixture was cooled, filtered and the filtrate was concentrated in vacuo to give ˜20 ml of solution. The concentrate was cooled and then filtered again. Ethanolic hydrogen chloride was added to the mother liquor, and the reaction mixture was concentrated to give a white solid, which was dissolved in water (15 ml). The solution was basified to pH 14 and the product was extracted with dichloromethane (7×50 ml). The extracts were dried, (Na2SO4) and concentrated to give the title compound as a yellowish residue, which was distilled to give the product (1.28 g, 7.0 mmol, 16%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07494992B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-5d00533441384f46bb124744605133f2 |
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| Source note | uspto-grants-2009_02 |
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