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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-tert-butoxycarbonylamino-N-benzylpropionamide | HCID 10850224 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Product | 3-amino-N-benzylpropanamide hydrochloride | HCID 51051959 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08048862B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-9cd6d3a500794cc19459d2813a76210f |
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| Source note | uspto-grants-2011_11 |
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