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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066084Generated: November 1, 2026

4-Hydroxybenzaldehyde → Benzaldehyde, 4-(2-hydroxyethoxy)-

https://huagongshe.com/reaction/2066084

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantEthanol, 1-bromo-HCID 14202443—
SolventDimethylformamideHCID 6228—
ProductBenzaldehyde, 4-(2-hydroxyethoxy)-HCID 8917880.2%

Reaction Steps

To a solution of 4-hydroxybenzaldehyde (366 mg, 3 mmol) in anhydrous DMF (7 ml), under nitrogen atmosphere, K2CO3 (829 mg, 6 mmol), and, after 10 minutes, bromoethanol (450 mg, 3.6 mmol) were added. The mixture was heated to reflux for 3 hours, then water was added and the product was extracted with CH2Cl2. The organic layers were washed with water and with NaCl saturated solution, dried with Na2SO4. After evaporation of the solvent, the crude product was purified by chromatography on silica gel (Petroleum ether/Ethyl acetate 2/1); 400 mg (yield 80%) of pure product of the title were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288528B2
Source datasetuspto-grants-2012_10
ORD IDord-13a82dcf1d5247d58a51f768766e578a
Source noteuspto-grants-2012_10