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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274919Generated: November 1, 2026

Glycinamide hydrochloride → HCID 11324179, compound

https://huagongshe.com/reaction/274919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycinamide hydrochlorideHCID 2723639—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 54026983HCID 54026983—
SolventMethanolHCID 887—
ProductHCID 11324179HCID 11324179—

Reaction Steps

22.4 g (0.203 mol) of glycinamide hydrochloride are suspended in 1000 ml of dry methanol and 10.2 g (0.162 mol) of sodium cyanoborohydride are added while stirring under nitrogen. After solubilization of the mixture, 50 g (0.203 mol) of 3-chlorobenzyloxybenzaldehyde are added in a single portion. The reaction mixture is stirred 8 hours at room temperature and then allowed to stand 16 hours. The solution is filtered and evaporated, taken up with water and extracted three times with methylene chloride. After drying and evaporating, the crude residue is chromatographed on silica gel (eluant: chloroform/methanol/conc. NH4OH; 97/3/0.3) to give 2-[4-(3-chlorobenzyloxy)benzyl]aminoacetamide which by reaction with the stoichiometric amount of gaseous HCl in ethanol is transformed into its hydrochloride (32.1 g, 46.3%, m.p.: 225°-230° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391577
Source datasetuspto-grants-1995_02
ORD IDord-07a2be9444b046b49e606272b265e802
Source noteuspto-grants-1995_02