HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615378Generated: October 30, 2026
4-Piperidone → 1-[(2,6-Dimethylphenyl)aminocarbonylmethyl]-4-piperidone
https://huagongshe.com/reaction/615378
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Piperidone | HCID 33721 | — |
| Reactant | 2-Chloro-N-(2,6-dimethylphenyl)acetamide | HCID 70798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[(2,6-Dimethylphenyl)aminocarbonylmethyl]-4-piperidone | HCID 13393353 | — |
Reaction Steps
The crude [(2,6-dimethylphenyl)aminocarbonylmethyl]chloride, prepared in Preparation B (50 g., 0.25 moles) and 4-piperidone (86 g, 1 mole) are dissolved in 500 ml of ethanol. The mixture is refluxed for two hours, and then cooled and evaporated. The product is recovered by adding aqueous ammonia to the residue, and extracting with methylene chloride. Three portions of methylene chloride are used, which are collected, washed with water, and evaporated to a semi-solid. Upon addition of diethylether, the product crystallizes and is filtered. The resulting crude mixture is boiled with ether and then evaporated to a residue and triturated with hexane to yield pure material, 1-[(2,6-dimethylphenyl)aminocarbonylmethyl]-4-piperidone. This material is of sufficient purity for use in Reaction Sequences 2 to 5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04499100 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-0839b93d1c3545e9a57da228cce56959 |
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| Source note | uspto-grants-1985_02 |
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