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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739404Generated: October 30, 2026

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

https://huagongshe.com/reaction/1739404

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantSodium hydrideHCID 24758—
ReactantHCID 21841067HCID 21841067—
SolventDimethylformamideHCID 6228—
Product4-(2-Phenoxyethoxy)benzaldehydeHCID 1348321664.4%

Reaction Steps

1.19 g of 4-hydroxybenzaldehyde were dissolved in 30 ml of DMF, and 0.41 g of 60% NaH were further added to the resultant solution while cooling it with ice. The solution was then stirred for 1 hour after elevating the temperature of the solution up to room temperature. The solution was again cooled with ice, then added with 2.0 g of 2-phenoxyethyl-methane sulfonate, and stirred for 1 hour at room temperature and subsequently for a night at 50-60° C. The solution reacted was poured into ice-water and extracted with ethyl acetate, then the organic layer resulted was dried with anhydrous magnesium sulfate. The solvent used was then removed by distillation under reduced pressure, and the residue obtained was washed with a mixture of ether and hexane, thereby affording 1.45 g of 4-(2-phenoxyethyloxy)benzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965743
Source datasetuspto-grants-1999_10
ORD IDord-2070c0609afe47438e3a39baf707cd68
Source noteuspto-grants-1999_10