HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459044Generated: October 29, 2026
N-Methyl-2-piperidone → 5-methylaminopentanoic Acid
https://huagongshe.com/reaction/459044
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methyl-2-piperidone | HCID 13603 | — |
| Reactant | Barium hydroxide | HCID 6093286 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-methylaminopentanoic Acid | HCID 11665412 | 83.4% |
Reaction Steps
1-methyl-2-piperidone (5 ml, 44.1 mmol) was combined with barium hydroxide (3.8 g, 26.95 mmol) and water (55 ml). The suspension was warmed to 110° C. for 6 hours then cooled over an ice bath. Gaseous carbon dioxide was bubbled through the solution for 20 minutes. The suspension was filtered through a celite pad and the filtrate was concentrated to dryness. The residue was triturated with acetonitrile, collected, rinsed with ether and dried in vacuo to yield 5-(methylamino)pentanoic acid as a white solid (2.95 g). 5-(Methylamino)pentanoic acid (2 g, 15.3 mmol), and potassium carbonate (13 g, 94 mmol) were suspended in water (30 ml) and dioxane (10 ml) then cooled to 0° C. Methyl chloroformate (5 ml, 65 mmol) was added over 30 seconds, then the mixture was stirred and allowed to warm slowly to room temperature for 16 hours. Conc. HCl (20 ml) was added then the mixture was diluted with water and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, evaporated and dried in vacuo to give 5-[(methoxycarbonyl)(methyl)amino]pentanoic acid as a thick clear oil (2.56 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192974B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-4f67bf12d3e84e1eaa12d1cdc1d5192d |
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| Source note | uspto-grants-2007_03 |
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