HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449492Generated: November 3, 2026
Chloroform → 1-(4-Bromobutyl)-2-piperidinone
https://huagongshe.com/reaction/1449492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 1,4-Dibromobutane | HCID 8056 | — |
| Reactant | 2-Piperidone | HCID 12665 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Bromobutyl)-2-piperidinone | HCID 536377 | 28% |
Reaction Steps
2-piperidone (1.98 g, 20.0 mmoles) was dissolved in 40 ml of dimethylformamide, 60% sodium hydride (840 mg, 21.0 mmoles) was added to the solution, and the mixture was stirred at 80° C. for 1 hour. After cooling the mixture to room temperature, 1,4-dibromobutane (21.6 g, 100 mmoles) was added, and the resulting mixture was stirred at room temperature for 12 hours. After chloroform was added to the reaction mixture, insolubles were removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was dissolved in chloroform and washed with water, and the solvent was evaporated. The residue was purified by chromatography on a silica gel column to give 1.30 g (yield 28%) of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05599815 |
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| Source dataset | uspto-grants-1997_02 |
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| ORD ID | ord-5947c882fbbd4de5b6aa47c338b74513 |
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| Source note | uspto-grants-1997_02 |
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