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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515089Generated: November 2, 2026

4-Hydroxybenzaldehyde → 4-[(2-methylbenzyl)oxy]benzaldehyde

https://huagongshe.com/reaction/1515089

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantWaterHCID 962—
Reactanto-Xylyl bromideHCID 6992—
ReactantCesium carbonateHCID 10796—
SolventDimethylformamideHCID 6228—
Product4-[(2-methylbenzyl)oxy]benzaldehydeHCID 2763432103%

Reaction Steps

4-Hydroxybenzaldehyde (10.0 g, 81.9 mmol) and 2-methyl benzyl bromide (40.0 g, 98.3 mmol) were dissolved in dimethylformamide (100 mL), and cesium carbonate (18.2 g, 123 mmol) was added thereto, and then, the resulting mixture was stirred under a nitrogen atmosphere at room temperature for 1 hour. Water was added to the reaction solution, and the organic matter was extracted with diethyl ether. The organic layer was washed with water and a saturated sodium chloride solution, then dried over anhydrous magnesium sulfate and filtered. Then, the solvent was distilled off under reduced pressure, whereby a crude product was obtained. This crude product was purified by silica gel column chromatography (hexane:ethyl acetate=100:0 to 60:40 (v/v)), whereby the objective title compound was obtained as a colorless oily substance (19.2 g, yield: 103%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222281B2
Source datasetuspto-grants-2012_07
ORD IDord-59ae6f86d281462fa067bc1f6676f0af
Source noteuspto-grants-2012_07