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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1647122Erstellt: 26. Oktober 2026

Tert-butyl (2S)-2-amino-3-[4-(tert-butoxy)phenyl]propanoate → Piperidine

https://huagongshe.com/reaction/1647122

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-butyl (2S)-2-amino-3-[4-(tert-butoxy)phenyl]propanoateHCID 7350495—
EduktN-[(9H-fluoren-9-yloxy)carbonyl]-3-(t-butoxycarbonyl)-L-alanineHCID 54139735—
ProduktPiperidineHCID 8082—
ProduktN-[N-[(9H-fluoren-9-yloxy)carbonyl]-3-(t-butoxycarbonyl)-L-alanyl]-3-(p-t-butoxyphenyl)-L-alanine t-butyl esterHCID 22849520—

Reaktionsschritte

N-[(9H-fluoren-9-yloxy)carbonyl]-3-(t-butoxycarbonyl)-L-alanine and 3-(p-t-butoxyphenyl)-L-alanine t-butyl ester were coupled to give N-[N-[(9H-fluoren-9-yloxy)carbonyl] -3-(t-butoxycarbonyl)-L-alanyl]-3-(p-t-butoxyphenyl)-L-alanine t-butyl ester and 5 ml of piperidine and the reaction solution was evaporated. The residue was suspended in methanol and insoluble material was filtered off. The filtrate was evaporated and chromatographed on silica gel using ethyl acetate to yield 2 g of 3-(t-butoxyphenyl)-N-[3-(p-t-butoxy-carbonyl)-L-alanyl]-L-alanine t-butyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05430024
Quelldatensatzuspto-grants-1995_07
ORD IDord-7f5bcbe068aa4c0da47b21ff0835966c
Quellennotizuspto-grants-1995_07