Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 272790Erstellt: 26. Oktober 2026

Ammonium → (S)-2-Amino-3-[4-(tert-butoxy)phenyl]propanamide

https://huagongshe.com/reaction/272790

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniumHCID 223—
EduktPyridineHCID 1049—
EduktDi-tert-butyl dicarbonateHCID 90495—
EduktFmoc-L-Tyr(tBu)-OHHCID 10895791—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelDiethylamineHCID 8021—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt(S)-2-Amino-3-[4-(tert-butoxy)phenyl]propanamideHCID 1502431781%

Reaktionsschritte

N-Fmoc-O-tert-butyl-tyrosine (3.27 g, 7.12 mmol) was dissolved in dioxane (15 mL). Ammonium hydrogenocarbonate (732 mg, 9.26 mmol), di-tert-butyl-dicarbonate (2.02 g, 9.26 mmol) and pyridine (0.4 mL) were added and the mixture was stirred under nitrogen atmosphere at room temperature for 12 h. It was then diluted with ethyl acetate and the organic phase was washed with brine (2×), 5% sulfuric acid (1×) and brine again. It was dried over magnesium sulfate and concentrated. The crude thus obtained (3.17 g) was dissolved in dichloromethane (50 mL) and diethylamine (10 mL). The mixture was stirred at room temperature for 12 h, concentrated under reduced pressure and purified by flash chromatography with DCM/MeOH/NH4OH (95/5/1 then 90/10/1) to give 1.37 g of the desired compound (yield=81%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456201B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-b3ee7894533f4b548def05bd37831a88
Quellennotizuspto-grants-2008_11