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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906627Generated: October 26, 2026

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

https://huagongshe.com/reaction/1906627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(1-Cyano-3-Phenylpropyl)-L-Alanine BenzylesterHCID 13826599—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductN-(1-Ethoxycarbonyl-3-Phenylpropyl)-L-Alanine BenzylesterHCID 13345971—

Reaction Steps

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].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04652668
Source datasetuspto-grants-1987_03
ORD IDord-1baf1110c54740bcadf30185f0d12406
Source noteuspto-grants-1987_03