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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820003Generated: October 28, 2026

4-Hydroxybenzaldehyde → 2-(4-formylphenoxy)propanoic acid

https://huagongshe.com/reaction/1820003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-bromopropionateHCID 79040—
SolventEthanolHCID 702—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-(4-formylphenoxy)propanoic acidHCID 35173771.5%

Reaction Steps

A solution of ethyl 2-bromopropanoate (6.38 ml, 49.1 mmol), 4-hydroxybenzaldehyde (5.00 g, 40.9 mmol) and potassium carbonate (6.79 g, 49.1 mmol) in acetonitrile (25 ml) was stirred at 60° C. for 16 hrs. Ethyl acetate was added to the reaction mixture, and the mixture was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by alumina column chromatography (developing solvent; ethyl acetate) to give an oil. To a solution of the obtained oil (9.10 g, 40.9 mmol) in ethanol (200 ml) was added 1N aqueous sodium hydroxide solution (61.4 ml), and the mixture was stirred at room temperature for 16 hrs, and concentrated under reduced pressure. Ethyl acetate was added to the obtained residue. The mixture was washed with 1N hydrochloric acid and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the obtained redsidue was powderized with isopropyl ether to give the title compound (5.68 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601868B2
Source datasetuspto-grants-2009_10
ORD IDord-aac153821707468b83e96fbaab9fac5f
Source noteuspto-grants-2009_10