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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722447Generated: October 30, 2026

N-(4-Methoxybenzylidene)glycine methyl ester → N-((4-Methoxyphenyl)methyl)glycine methyl ester

https://huagongshe.com/reaction/722447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(4-Methoxybenzylidene)glycine methyl esterHCID 4193973—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductN-((4-Methoxyphenyl)methyl)glycine methyl esterHCID 10846084—

Reaction Conditions

Temperature-5 °C

Reaction Steps

To a solution of 91.3 g (0.441 mol) of [(4-methoxy-benzylidene)-amino]-acetic acid methyl ester in 500 ml of THF and 1000 ml of MeOH, 20 g (0.529 mol) of sodium borohydride is added portionwise at −10 to 0° C. The reaction mixture is stirred for 30 min. at −10 to 0° C. and quenched with sat. NH4Cl. After adding of ice-water, the mixture is concentrated to ¼ of whole volume and extracted with AcOEt. The combined extracts are washed with H2O and brine, dried over MgSO4 and concentrated under reduced pressure to give (4-methoxybenzylamino)-acetic acid methyl ester; NMR (CDCl3): 1.87 (br s, 1H), 3.41 (s, 2H), 3.73 (s, 3H), 3.74 (s, 2H), 3.8 (s, 3H), 6.86 (d, 2H, J=8.56 Hz), 7.24 (d, 2H, J=8.56 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138432B1
Source datasetuspto-grants-2006_11
ORD IDord-a9b116057f5043d9acdbe7f7a69de1ee
Source noteuspto-grants-2006_11