Reaktion #6534

Reaktionsgleichung

Phenylacetone

Beta-alanine

sodium cyanoborohydride

→

N-carboxyethyl-amphetamine

Ausbeute 60.2%

Lösungsmittel

methanol

ethyl acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   Filtrationthe reaction mixture was filtered
2. 2
   Sonstigethe filtrate solvent was removed in vacuo
3. 3
   SonstigeThe resulting crude material was purified on four 1.0 millimeter C18 reverse-phase preparative thin layer chromatography plates
4. 4
   Wascheneluted with H2O/methanol/acetic acid (40/60/0.4)
5. 5
   SonstigeThe material obtained
6. 6
   Extraktionwas extracted with 1.0M sodium bicarbonate (3×20 ml)
7. 7
   Sonstigethe solvent was removed in vacuo
8. 8
   SonstigeThe resulting crystalline solid was then triturated twice with 50-milliliter portions of ethyl acetate
9. 9
   Filtrationfiltered
10. 10
    Sonstigethe solvent was removed in vacuo

Vorschrift

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.

Quelle