HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038557Generated: November 1, 2026
Benzyl Bromide → (S)-methyl 2-(benzylamino)propanoate
https://huagongshe.com/reaction/1038557
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Alanine methyl ester hydrochloride | HCID 2733257 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-methyl 2-(benzylamino)propanoate | HCID 10535780 | 61.4% |
Reaction Steps
L-alanine methyl ester hydrochloride (15.0 g, 107 mmol) was dissolved in N,N′-dimethylformamide (150 mL), added potassium carbonate (32.5 g, 235 mmol) and benzyl bromide (18.4 g, 107 mmol) and the mixture was stirred at 80° C. overnight. Then, the mixture was reverted to room temperature, the reaction solution was filtered through a pad of celite, extracted with ethyl acetate, washed with water and brine, dried over sodium sulfate, and concentrated in vacuo. The obtained residue was purified by silica-gel column chromatography (hexane/ethyl acetate), and the title compound (12.7 g, 61%) was obtained as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08551985B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-f0757a9e1f7943aea966d1074ecc9a34 |
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| Source note | uspto-grants-2013_10 |
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