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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642026Generated: October 31, 2026

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

https://huagongshe.com/reaction/1642026

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPotassium CarbonateHCID 11430—
ReactantEthanol, 2-methoxy-, 1-(4-methylbenzenesulfonate)HCID 86977—
SolventDimethyl SulfoxideHCID 679—
Product4-(2-Methoxyethoxy)benzaldehydeHCID 648556098.8%

Reaction Steps

A solution of 5.0 grams (0.041 mole) of 4-hydroxybenzaldehyde, 9.5 grams (0.041 mole) of p-toluene sulfonic acid 2-methoxyethyl ester, and 6.3 grams (0.046 mole) of anhydrous potassium carbonate in 50 mL of dimethylsulfoxide (DMSO) was stirred at ambient temperature for about 72 hours. The reaction mixture was then partitioned between 300 mL of an aqueous mixture of 10% lithium chloride and 100 mL of ethyl acetate. The ethyl acetate portion was washed three times; first, with 100 mL of an aqueous mixture of 10% sodium hydroxide, second, with 100 mL of an aqueous mixture of 10% lithium chloride, and, third, with 100 mL of brine. The resultant organic layer was dried over magnesium sulfate, filtered and concentrated under reduced pressure to a residue. The residue was purified with column chromatography on silica gel using methylene chloride as an eluant. The appropriate fractions were combined and concentrated under reduced pressure, yielding 7.3 grams of the subject compound. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119563B2
Source datasetuspto-grants-2012_02
ORD IDord-f971c7f6d6b446c9a374c842aed67555
Source noteuspto-grants-2012_02