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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1906628Erstellt: 26. Oktober 2026

N-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine Benzylester → N-(1-ethoxycarbonyl-3-phenylpropyl)-L-alanine

https://huagongshe.com/reaction/1906628

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine BenzylesterHCID 13345971—
EduktHCID 178418361HCID 178418361—
KatalysatorAcetic AcidHCID 176—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
ProduktN-(1-ethoxycarbonyl-3-phenylpropyl)-L-alanineHCID 13044262—

Reaktionsschritte

N-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine Benzylester (4.2 g) is dissolved in 40 ml ethanol, to which is added 630 mg 10% Pd-C and a few drops of acetic acid. Hydrogenation occurs under a 30 psi hydrogen atmosphere at room temperature overnight. The resulting mixture is filtered through celite and dried under vacuum to remove the solvent, yielding a residue. The residue is partitioned between chloroform and aqueous 5% NaHCO3, separated, and the chloroform layer further washed with aqueous 5% NaHCO3. The aqueous layers are combined, acidified to pH 3.5 with dilute HCl, extracted with chloroform or ethylacetate several times, dried over MgSO4, and placed under vacuum to evaporate the solvent and yield 2.5 g of the diastereoisomeric product, a brown sticky solid [TLC (Silica gel; CHCl3 /MeOH/HOAC=9:1:0.5); Rf=0.4].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04652668
Quelldatensatzuspto-grants-1987_03
ORD IDord-b0927fd42b5647caac7d9bc33a5eef9a
Quellennotizuspto-grants-1987_03