HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274919Generated: October 31, 2026
Glycinamide hydrochloride → HCID 11324179, compound
https://huagongshe.com/reaction/274919
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycinamide hydrochloride | HCID 2723639 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 54026983 | HCID 54026983 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 11324179 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05391577 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-07a2be9444b046b49e606272b265e802 |
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| Source note | uspto-grants-1995_02 |
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