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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4981Erstellt: 23. Oktober 2026

Hydrochloric Acid → Ac-Ala-Lys(Boc)-OH

https://huagongshe.com/de/reaction/4981

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethylamineHCID 8471—
EduktSodium HydroxideHCID 14798—
EduktN-HydroxysuccinimideHCID 80170—
EduktN-Acetyl-L-alanineHCID 88064—
Edukt(2S)-2-amino-6-(((tert-butoxy)carbonyl)amino)hexanoic acidHCID 2733283—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktAc-Ala-Lys(Boc)-OHHCID 131717743—

Reaktionsschritte

Ac-Ala-Lys(Boc)-OH was prepared by coupling the N-hydroxysuccinimide ester of Ac-Ala-OH, prepared by the method of Anderson et al., J. Am. Chem. Soc. 86: 1839, (1964), to H-Lys(Boc)-OH. The N-hydroxy-succinimide of Ac-Ala-OH (6.25 g, 27.4 mmoles) was dissolved in 30 mL of dioxane and was added to a solution of H-Lys(Boc)-OH (7.50 g, 30.4 mmoles) dissolved in a solution consisting of 30 mL of 1.0N sodium hydroxide and triethylamine (2.12 mL, 15.0 mmoles). The reaction mixture was stirred overnight, then acidified with hydrochloric acid. Sufficient dry sodium chloride to nearly saturate the solution was added. The product was extracted into ethyl acetate and it was washed with 0.2N hydrochloric acid prepared in saturated aqueous sodium chloride. The organic phase was dried over anhydrous sodium sulfate and filtered. Solvent was removed by evaporation. The product was crystallized from ethyl acetate:hexane to yield 7.3 g (mp 86°-89°).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05242904
Quelldatensatzuspto-grants-1993_09
ORD IDord-408c8484fe124834b5520e846e9adf68
Quellennotizuspto-grants-1993_09