HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553460Generated: October 26, 2026
Benzylamine → 3-tert-butoxycarbonylamino-N-benzylpropionamide
https://huagongshe.com/reaction/553460
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-((1,1-dimethylethoxy)carbonyl)-beta-alanine | HCID 76809 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Solvent | Dioxane methylene chloride | HCID 18626912 | — |
| Product | 3-tert-butoxycarbonylamino-N-benzylpropionamide | HCID 10850224 | 82% |
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-081afe95e6734940bcb30313933b840c |
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| Source note | uspto-grants-2011_11 |
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