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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720590Generated: November 4, 2026

Benzaldehyde → methyl (2R)-2-(benzylamino)propanoate

https://huagongshe.com/reaction/1720590

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethyl D-alaninate hydrochlorideHCID 11182647—
SolventMethanolHCID 887—
Productmethyl (2R)-2-(benzylamino)propanoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506242
Source datasetuspto-grants-1996_04
ORD IDord-d2417f799cea41f29e208900e3a48fc5
Source noteuspto-grants-1996_04