HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156773Generated: October 30, 2026
1,4-Dichlorobutane → HCID 12855246, compound
https://huagongshe.com/reaction/1156773
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4-Dichlorobutane | HCID 8059 | — |
| Reactant | 2-Piperidone | HCID 12665 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 12855246 | HCID 12855246 | — |
Reaction Steps
Sodium hydride (3.87 g of 50% dispersion in oil, 0.0807 mole) was suspended and stirred in 80 ml of dry dimethylformamide. A solution of 1,4-dichlorobutane (44 ml, 0.404 mole) and 2-piperidone (8 g, 0.0807 mole) in 100 ml of dimethylformamide was added dropwise over 1 hour, maintaining the temperature at 25°-30° C. by use of a water bath. The reaction mixture was stirred for 16 hours at room temperature, then byproduct salt removed by filtration and the mother liquor evaporated in vacuo to one-tenth volume. The resulting concentrate was distributed between 100 ml of water and 100 ml of hexane. The lower, oily phase of three phases was separated, diluted with 50 ml of methylene chloride, dried over magnesium sulfate, filtered and evaporated to yield 1-(4-chloro-1-butyl)-2-piperidone as an oil [14.3 g; pnmr(CDCl3) delta 1.4-1.83 (4H, m), 3.03-3.72 (6H, m), 4.10-4.43 (2H, t, J=7)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04337250 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-7a65351ba4bc4cbeb67e6a94ac266793 |
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| Source note | uspto-grants-1982_06 |
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