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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992717Generated: November 2, 2026

4-Hydroxybenzaldehyde → Ethyl 2-(4-formylphenoxy)acetate

https://huagongshe.com/reaction/992717

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantIodineHCID 807—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductEthyl 2-(4-formylphenoxy)acetateHCID 291358—

Reaction Steps

4-Hydroxybenzaldehyde (250 g, 2.05 M), potassium carbonate (565 g, 4.09 M), toluene (2.5 L), p-toluene sulphonic acid (39 g, 0.21 M) and iodine (2 g, catalytic) were taken in a 5 L 4-neck round bottom flask with mechanical stirrer and a Dean-Stark condenser. Ethylbromoacetate (341 g, 2.05 M) was added and the reaction refluxed for 6-8 hours, under azeotropic removal of water, while monitoring the reaction on TLC. After the completion of the reaction, water was added and the organic layer separated while the aq. layer was extracted with toluene (2×500 ml). The combined organic layers were washed with brine and concentrated under vacuum to yield 4-((carboethoxy)methoxy)benzaldehyde as an oily material (407 g, Y=96%, P=99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06469167B1
Source datasetuspto-grants-2002_10
ORD IDord-5b23d4e8f5de4f6c9c02e8e2fe1ff3d1
Source noteuspto-grants-2002_10