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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992720Generated: November 2, 2026

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

https://huagongshe.com/reaction/992720

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantIodineHCID 807—
ReactantMethanesulfonic AcidHCID 6395—
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), methanesulfonic acid (20 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 was 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 (400 g, Y=94%, P=99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06469167B1
Source datasetuspto-grants-2002_10
ORD IDord-c9edbe27106f43efac12f19111d0655c
Source noteuspto-grants-2002_10