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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299741Generated: October 26, 2026

4-Hydroxybenzaldehyde → 4-Methoxymethoxybenzylalcohol

https://huagongshe.com/reaction/2299741

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantDimethylformamideHCID 6228—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantPotassium CarbonateHCID 11430—
SolventWaterHCID 962—
SolventEthyl acetate hexaneHCID 21226206—
Product4-MethoxymethoxybenzylalcoholHCID 1160798482%

Reaction Steps

Chloromethyl methyl ether (34.2 ml) was added to a mixture of 4-hydroxybenzaldehyde (50.0 g), potassium carbonate (84.9 g) and N,N-dimethylformaldehyde (150 ml) at 0° C. and stirred at room temperature for 11 hours. Water was added to the reaction mixture and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was dissolved in tetrahydrofuran (300 ml) and methanol (50 ml) and sodium borohydride (7.76 g) was added in portions at 0° C. After stirring for 30 minutes, water was added to the reaction mixture and extracted with ethyl acetate. The ethyl acetate layer was washed with an aqueous saturated solution of sodium chloride, dried (MgSO4) and concentrated. The residue was subjected to silica gel chromatography to obtain 4-methoxymethoxybenzylalcohol (56.7 g, yield 82%) as a colorless oil from an ethyl acetate-hexane (2:3, v/v) eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495581B1
Source datasetuspto-grants-2002_12
ORD IDord-1fc1bbeda2614def9e66285122d34575
Source noteuspto-grants-2002_12