HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402267Generated: October 29, 2026
2-Piperidone → 1-(4-Methoxybenzyl)piperidin-2-one
https://huagongshe.com/reaction/402267
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Piperidone | HCID 12665 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-Methoxybenzyl)piperidin-2-one | HCID 11506801 | 52.1% |
Reaction Steps
A suspension of potassium hydroxide (85%, 18.6 g) and tetrabutylammonium bromide (4.88 g) in toluene (250 ml) was refluxed overnight under nitrogen atmosphere using Deenschtark device. The mixture was cooled to 80° C., to which a solution of 2-piperidone (25.0 g) and 4-methoxybenzylchloride (51.3 g) in toluene (50 ml) were added dropwise. After refluxing for 8 hours, the reaction mixture was returned to room temperature and washed with water and saturated brine. The resultant was dried with magnesium sulfate, after which the solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane ethyl acetate=1:1) to give 1-(4-methoxybenzyl)piperidin-2-one (28.8 g) as a colorless oily material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741943B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-9d2bd276c5154b68a6d96b3bb8cddab3 |
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| Source note | uspto-grants-2014_06 |
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