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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362068Generated: October 27, 2026

4-Methoxybenzaldehyde → N-[(4-Methoxyphenyl)methyl]glycine ethyl ester

https://huagongshe.com/reaction/1362068

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzaldehydeHCID 31244—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventMethanolHCID 887—
ProductN-[(4-Methoxyphenyl)methyl]glycine ethyl esterHCID 1173621249%

Reaction Steps

A suspension of glycine ethyl ester hydrochloride (10.0 g, 71.6 mmol) and NaBH3CN (5.00 g, 79.6 mmol) in MeOH (60 mL) was treated dropwise over 15 min with p-anisaldehyde (11.0 mL, 90.4 mmol). After stirring at room temperature overnight, the solvent was removed in vacuo. The residue was partitioned between CH2Cl2 (200 mL) and saturated aqueous NaHCO3 (300 mL). The aqueous layer was extracted with CH2Cl2 (2×200 mL) and the combined organic layers were washed with brine, dried over Na2SO4, filtered and the solvent was removed in vacuo. Purification by flash column chromatography (silica gel, hexanes/EtOAc, 90:10 to 50:50) gave the title compound (7.77 g, 49%) as a colorless liquid: MS (ESI) m/e 224 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879872B2
Source datasetuspto-grants-2011_02
ORD IDord-6d71abff6e2f47778083623e55d2f054
Source noteuspto-grants-2011_02