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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 223103Erstellt: 24. Oktober 2026

Trifluoroacetic acid → L-Phenylalanyl-L-alanine

https://huagongshe.com/de/reaction/223103

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
Edukt1-(1(S)-t-butoxycarbonylethyl)-3(S)-azido-4(R)-phenylazetidin-2-oneHCID 13035214—
KatalysatorPalladiumHCID 23938—
ProduktTrifluoroacetic acidHCID 6422—
ProduktL-Phenylalanyl-L-alanineHCID 548819694%

Reaktionsschritte

After 1-(1(S)-t-butoxycarbonylethyl)-3(S)-azido-4(R)-phenylazetidin-2-one (300 mg., 0.95 mmol) was stirred in trifluoroacetic acid (2 ml.) at room temperature for 15 hours, the solvent was removed by distillation under reduced pressure. The thus obtained oil (360 mg.) was hydrogenated in 25 ml. of ethanol at 50° C. for 15 hours under ambient pressure using a 10% Pd-C (300 mg.) as a catalyst to give trifluoroacetic acid salt of L-phenylalanyl-L-alanine (311 mg., yield: 94%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04352752
Quelldatensatzuspto-grants-1982_10
ORD IDord-8446506b615d4f04850806817179a906
Quellennotizuspto-grants-1982_10