HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576533Generated: October 25, 2026
1-Phenyl-2-propen-1-one → 1,3-Dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-one
https://huagongshe.com/reaction/576533
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Phenyl-2-propen-1-one | HCID 13028 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 1,3-Dimethyl-4-piperidone | HCID 107311 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-one | HCID 67357110 | 10.8% |
Reaction Steps
To a stirred solution of 1,3-dimethyl-piperidin-4-one (0.1 g, 0.787 mmol) in mixture of 1,4 dioxane (2 mL) and water (0.1 mL) was added crushed KOH (44 mg, 0.787 mmol). The reaction mixture was stirred at 25° C. for 10 min. To this was added 1-phenylprop-2-en-1-one (103 mg, 0.787 mmol) dropwise. The reaction mixture was stirred at 25° C. for 2 h. The reaction mixture was concentrated under reduced pressure and the residue was diluted with water (10 mL) and EtOAc (20 mL), the organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The resulting crude product was purified by column chromatography on neutral alumina (eluted with EtOAc:Hexanes, 1:99) to afford 1,3-dimethyl-3-(3-oxo-3-phenyl-propyl)-piperidin-4-one as an oil (22 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040519B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-0c551d20fef6440ca1f200327530665c |
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| Source note | uspto-grants-2015_05 |
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