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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245381Generated: October 25, 2026

4-Hydroxybenzaldehyde → 4-(2-Methyl-quinolin-4-ylmethoxy)-benzaldehyde

https://huagongshe.com/reaction/1245381

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Chloromethyl)-2-methylquinolineHCID 11535719—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-(2-Methyl-quinolin-4-ylmethoxy)-benzaldehydeHCID 2191116690%

Reaction Steps

p-Hydroxybenzaldehyde (3.18 g, 26.1 mmol), 4-chloromethyl-2-methyl-quinoline (5.0 g, 26.1 mmol), and potassium carbonate (7.2 g, 52 mmol) were combined in acetonitrile (100 mL) and heated to reflux overnight. The reaction was allowed to cool to room temperature, diluted with ethyl acetate, filtered to remove the solids, and concentrated to give a semi-solid residue. The crude product was crystallized from ethyl ether to give 4-(2-methyl-quinolin-4-ylmethoxy)-benzaldehyde (6.5 g, 90%) as an off white precipitate. MS found: (M+H)+=278.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125870B2
Source datasetuspto-grants-2006_10
ORD IDord-8004bc2841974ee6a4fe0f8d6277fcbf
Source noteuspto-grants-2006_10