HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264295Generated: October 26, 2026
Benzaldehyde → methyl (2R)-2-(benzylamino)propanoate
https://huagongshe.com/reaction/264295
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Methyl D-alaninate hydrochloride | HCID 11182647 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | methyl (2R)-2-(benzylamino)propanoate | HCID 10987118 | — |
Reaction Steps
To a solution of D-alanine methyl ester hydrochloride (3.0 g, 21.5 mmol) in methanol (10 mL) is added benzaldehyde (2.3 mL, 22.6 mmol). The reaction mixture is stirred at room temperature for 3 hours. The solvent is then evaporated. To the resultant residue is added acetic acid (15 mL) and methanol (1 mL) followed by portionwise addition of sodium cyanoborohydride (1.35 g, 21.5 mmol) at room temperature. The mixture is stirred overnight, and then the solvent is evaporated. The remaining residue is diluted with water (75 mL) and basified with Na2CO3. The mixture is extracted with ethyl acetate (3×75 mL). The combined organic extracts are washed with brine (50 mL), dried (Na2SO4), and the solvent is evaporated to give N-benzyl-D-alanine methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646167 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-1e2135e7b33748c5989125d07bdcebe3 |
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| Source note | uspto-grants-1997_07 |
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