Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl chloroformateHCID 6586—
ReactantPotassium CarbonateHCID 11430—
Reactant5-methylaminopentanoic AcidHCID 11665412—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-[(Methoxycarbonyl)(methyl)amino]pentanoic acidHCID 1844297388.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192974B2
Source datasetuspto-grants-2007_03
ORD IDord-82314f049a1c4ca38f9101eba94e3c7a
Source noteuspto-grants-2007_03