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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553460Generated: October 26, 2026

Benzylamine → 3-tert-butoxycarbonylamino-N-benzylpropionamide

https://huagongshe.com/reaction/553460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-((1,1-dimethylethoxy)carbonyl)-beta-alanineHCID 76809—
ReactantN-HydroxysuccinimideHCID 80170—
SolventDioxane methylene chlorideHCID 18626912—
Product3-tert-butoxycarbonylamino-N-benzylpropionamideHCID 1085022482%

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-081afe95e6734940bcb30313933b840c
Source noteuspto-grants-2011_11