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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553461Generated: November 1, 2026

3-tert-butoxycarbonylamino-N-benzylpropionamide → 3-amino-N-benzylpropanamide hydrochloride

https://huagongshe.com/reaction/553461

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-tert-butoxycarbonylamino-N-benzylpropionamideHCID 10850224—
ReactantHydrochloride methanolHCID 21893726—
Product3-amino-N-benzylpropanamide hydrochlorideHCID 51051959100%

Reaction Steps

A solution of 3-tert-butoxycarbonylaminopropanoic acid (2 g, 10.6 mmol.) and HOSu (1.22 g, 10.6 mmol.) in 40 mL DCM/Dioxane (2:1) was cooled in an ice bath. To this solution was added DCC (2.4 g, 11.6 mmol.), and the mixture was stirred at room temperature for 1 h. To the resulting mixture was added benzylamine (1.7 g, 15.8 mmol.), the mixture was stirred for 4 h at room temperature. The solid that formed in the mixture was removed by filtration and washed with EtOAc. The filtrate and washings were combined and washed with 1N HCl and saturated aqueous NaHCO3. The organic layer was dried over Na2SO4, filtered and concentrated to afford 3-tert-butoxycarbonylamino-N-benzylpropionamide (2.4 g, 82%). 3-tert-Butoxycarbonylamino-N-benzylpropionamide was dissolved in cooled HCl/MeOH (20 mL) and the resulting mixture was stirred at room temperature for 1.5 h. The solvent was removed to afford 3-amino-N-benzylpropionamide hydrochloride (1.8 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048862B2
Source datasetuspto-grants-2011_11
ORD IDord-9cd6d3a500794cc19459d2813a76210f
Source noteuspto-grants-2011_11