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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275893Generated: October 25, 2026

3-Ethoxy-4-methoxybenzaldehyde → 3-(3-Ethoxy-4-methoxy-benzylamino)-propionic acid ethyl ester

https://huagongshe.com/reaction/275893

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Ethoxy-4-methoxybenzaldehydeHCID 244728—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventEthanolHCID 702—
Product3-(3-Ethoxy-4-methoxy-benzylamino)-propionic acid ethyl esterHCID 5385854439.1%

Reaction Steps

A mixture of β-alanine ethyl ester hydrochloride (1.6 g), 3-ethoxy-4-methoxybenzaldehyde (1.8 g), sodium cyanoborohydride (0.42 g) and powdered 3Å molecular seives (2.5 g) in ethanol (25 ml) was stirred at ambient temperature for 24 hours. A further aliquot of sodium cyanoborohydride (0.42 g) was added and stirring was continued for a further 24 hours. The reaction mixture was filtered and the filtrate was evaporated. The residue was treated with ethyl acetate (100 ml) and the solution was washed with 10% aqueous potassium carbonate (50 ml), then twice with water (25 ml), then with brine (25 ml), then dried over magnesium sulphate and then evaporated. The residual oil was subjected to flash chromatography on silica eluting with a mixture of dichloromethane and methanol (95:5, v/v) to give the title compound as a colourless oil (1.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06352977B1
Source datasetuspto-grants-2002_03
ORD IDord-63a853df8ade4b968ea2376812013b75
Source noteuspto-grants-2002_03