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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1906627Erstellt: 27. Oktober 2026

Hydrochloric Acid → N-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine Benzylester

https://huagongshe.com/reaction/1906627

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthanolHCID 702—
EduktWaterHCID 962—
EduktSodium BicarbonateHCID 516892—
EduktN-(1-Cyano-3-Phenylpropyl)-L-Alanine BenzylesterHCID 13826599—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine BenzylesterHCID 13345971—

Reaktionsschritte

N-(1-Cyano-3-Phenylpropyl)-L-Alanine Benzylester (4.24 g) is then dissolved in 65 ml dry dichloromethane and diluted with 2.39 g absolute ethanol. After cooling on ice, the solution is saturated with dry HCl, stored for 2 days at 0°-5° C., and evaporated to form a residue which is dissolved in 30 ml of a 2:1 acetonitrile:water mixture at room temperature for 15 minutes. An excess of aqueous NaHCO3 is then added to the mixture, which is extracted with chloroform several times, dried over MgSO4, and placed under vacuum to evaporate the solvent, yielding N-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine Benzylester [TLC (Silica gel; CHCl3 /acetone=9:1); Rf=0.60].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04652668
Quelldatensatzuspto-grants-1987_03
ORD IDord-1baf1110c54740bcadf30185f0d12406
Quellennotizuspto-grants-1987_03