HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459045Generated: October 29, 2026
Hydrochloric Acid → 5-[(Methoxycarbonyl)(methyl)amino]pentanoic acid
https://huagongshe.com/reaction/459045
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-methylaminopentanoic Acid | HCID 11665412 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-[(Methoxycarbonyl)(methyl)amino]pentanoic acid | HCID 18442973 | 88.4% |
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-82314f049a1c4ca38f9101eba94e3c7a |
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| Source note | uspto-grants-2007_03 |
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