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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992722Generated: November 1, 2026

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

https://huagongshe.com/reaction/992722

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantIodineHCID 807—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantMethyl chloroacetateHCID 7295—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductMethyl 2-(4-formylphenoxy)acetateHCID 758214—

Reaction Steps

4-Hydroxybenzaldehyde (250 g, 2.05 M), potassium carbonate (565 g, 4.09 M), toluene (2.5 L), p-toluenesulfonic 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. Methylchloroacetate (233 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-((carbomethoxy)methoxy)benzaldehyde as an oily material (380 g, Y=95%, P=99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06469167B1
Source datasetuspto-grants-2002_10
ORD IDord-aa294fa12b4640939cdf4d056d8e5537
Source noteuspto-grants-2002_10