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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595371Generated: November 4, 2026

4-Hydroxybenzaldehyde → 4-(2-Methoxyethoxy)benzaldehyde

https://huagongshe.com/reaction/1595371

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloroethyl methyl etherHCID 12316—
SolventDimethylformamideHCID 6228—
Product4-(2-Methoxyethoxy)benzaldehydeHCID 648556047.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

4-Hydroxybenzaldehyde (300 g) and 2-chloroethyl methyl ether (279 g) were dissolved in DMF (3 L) and potassium carbonate (408 g) was added. The mixture was stirred with heating at 60° C. for 16 hr. After the reaction, the reaction mixture was poured into water and liberated oil was extracted with ethyl acetate. The organic layer was washed with 1N aqueous sodium hydroxide solution and washed with saturated brine. The organic layer was dried over anhydrous magnesium sulfate. After drying, the residue was concentrated under reduced pressure to give 4-(2-methoxyethoxy)benzaldehyde as an oil (212 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288061B1
Source datasetuspto-grants-2001_09
ORD IDord-d6a7c5e238a047bc968413ed9a66a171
Source noteuspto-grants-2001_09