Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254682Generated: November 1, 2026

Glycinamide hydrochloride → HCID 11324179, compound

https://huagongshe.com/reaction/2254682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycinamide hydrochlorideHCID 2723639—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-(Benzyloxy)-3-chlorobenzaldehydeHCID 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-chlorobenzyl)oxybenzyl] 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 numberUS05236957
Source datasetuspto-grants-1993_08
ORD IDord-b2815b51599b425ebb4536ee1092c36c
Source noteuspto-grants-1993_08