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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369422Generated: October 27, 2026

4-Hydroxybenzaldehyde → 4-(2-quinolinylmethoxy)Benzaldehyde

https://huagongshe.com/reaction/369422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethyl)quinoline hydrochlorideHCID 3083823—
SolventDimethylformamideHCID 6228—
Product4-(2-quinolinylmethoxy)BenzaldehydeHCID 1457896091%

Reaction Conditions

Temperature90 °C

Reaction Steps

2-Chloromethylquinoline hydrochloride (6.42 g, 30 mmol), 4-hydroxybenzaldehyde (3.66 g, 30 mmol) and potassium carbonate (9.12 g, 66 mmol) were combined, to which 50 ml of DMF were added. The resulting mixture was stirred overnight at 90° C. The solvent was driven off under reduced pressure, the residue was extracted with ethyl acetate. The organic layer was washed with 1 N aqueous solution of sodium hydroxide and a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure, whereby 7.19 g of the title compound were obtained (yield: 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136848
Source datasetuspto-grants-2000_10
ORD IDord-5f7fe61a123447d3aa0c0d1a7700f7ac
Source noteuspto-grants-2000_10