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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 6438Erstellt: 23. Oktober 2026

Beta-Alanine → N-carboxyethyl-amphetamine

https://huagongshe.com/de/reaction/6438

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
PatentnummerUS05248791
Quelldatensatzuspto-grants-1993_09
ORD IDord-478badbfe80b4ba79d32c3a102b14cc6
Quellennotizuspto-grants-1993_09