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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2372880Erstellt: 24. Oktober 2026

Beta-Alanine → N-carboxyethyl-amphetamine

https://huagongshe.com/de/reaction/2372880

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBeta-AlanineHCID 239—
EduktPhenylacetoneHCID 7678—
EduktSodium cyanoborohydrideHCID 5003444—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-carboxyethyl-amphetamineHCID 1446324360,2%

Reaktionsschritte

Phenylacetone (100 mg, 0.745 mmol) was dissolved in anhydrous methanol (2.0 ml). Beta-alanine (398 mg, 4.47 mmol) was added, followed by sodium cyanoborohydride (94 mg, 1.49 mmol). After 18 hours of stirring under nitrogen, the reaction mixture was filtered, and the filtrate solvent was removed in vacuo. The resulting crude material was purified on four 1.0 millimeter C18 reverse-phase preparative thin layer chromatography plates eluted with H2O/methanol/acetic acid (40/60/0.4). The material obtained was dissolved in ethyl acetate (20 ml) and was extracted with 1.0M sodium bicarbonate (3×20 ml). The aqueous extracts were combined, the pH was adjusted to 4 with 1.0M hydrochloric acid, and the solvent was removed in vacuo. The resulting crystalline solid was then triturated twice with 50-milliliter portions of ethyl acetate and filtered. The filtrates were combined, and the solvent was removed in vacuo to yield 93 milligrams of N-carboxyethyl-amphetamine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05101015
Quelldatensatzuspto-grants-1992_03
ORD IDord-672d7e4cf34d4e9999d8f5472e7f45ad
Quellennotizuspto-grants-1992_03