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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746088Generated: November 1, 2026

4-Hydroxybenzaldehyde → Benzaldehyde, 4-[(2-methoxyethoxy)methoxy]-

https://huagongshe.com/reaction/1746088

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
SolventAcetoneHCID 180—
ProductBenzaldehyde, 4-[(2-methoxyethoxy)methoxy]-HCID 1140156180%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Methoxyethoxymethyl chloride (5.10 mL, 45.0 mmol) was slowly added to a mixture of 4-hydroxybenzaldehyde (5.00 g, 40.9 mmol) and K2CO3 (6.20 g, 45.0 mmol) in acetone (70 mL) cooled at 0° C. The mixture was allowed to reach room temperature and stirred for 40 h. After removal of the solvent, the crude residue was dissolved in EtOAc (50 mL) and consecutively washed with water (50 mL) and NaOH (10% aqueous solution, 2×20 mL). The organic layer was dried over anhydrous Na2SO4 and filtered. After removal of the solvent, 6.85 g of 4-((2-methoxyethoxy)methoxy)benzaldehyde were obtained [Rf=0.6 (50% AcOEt/Hexanes), colorless oil, 80% yield], that were used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09149447B2
Source datasetuspto-grants-2015_10
ORD IDord-7c5100dcbe8d41a9aa3ced61b76ea555
Source noteuspto-grants-2015_10