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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729012Generated: October 30, 2026

Hydrochloric Acid → HCID 54003055, compound

https://huagongshe.com/reaction/729012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantEthyl 3-aminopropanoateHCID 419889—
Reactant2-(Oxiran-2-ylmethoxy)benzonitrileHCID 12619671—
SolventEthanolHCID 702—
ProductHCID 54003055HCID 54003055—

Reaction Steps

15.36 g of the hydrochloride of ethyl 3-aminopropanoate and 6.2 g of potassium hydroxide were stirred in 150 ml of abs. ethanol until neutral reaction, ca 1 h. Under reflux was added 8.7 g of 2-(2,3-epoxypropoxy)benzonitrile in 125 ml of abs. ethanol. The mixture was refluxed for 8 h, filtered and evaporated. The residue was dissolved in ether, washed twice with water and extracted with 25 ml of 2-n hydrochloric acid. The aqueous phase was extracted with methylene chloride. The methylene chloride phase was dried over Na2SO4, filtered and evaporated to dryness. The hydrochloride of ethyl N-[3-(2-cyanophenoxy)-2-hydroxypropyl]-3-aminopropanoate crystallized. Yield 5.75 g. Melting point 120° C. (HCl). The structure was determined using NMR and equivalent weight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05051446
Source datasetuspto-grants-1991_09
ORD IDord-cc46c5ec84a14c2caee42c63827d47f9
Source noteuspto-grants-1991_09