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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811397Generated: October 27, 2026

Dimethylformamide → 1-(4-Chlorobenzyl)-2-oxo-1,2-dihydroquinoline-3-carboxaldehyde

https://huagongshe.com/reaction/1811397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant1-(Bromomethyl)-4-chlorobenzeneHCID 69329—
Reactant2-Hydroxyquinoline-3-carbaldehydeHCID 589334—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product1-(4-Chlorobenzyl)-2-oxo-1,2-dihydroquinoline-3-carboxaldehydeHCID 8661391674.5%

Reaction Steps

Sodium hydride (60% in oil) (1.3 g) was added at 0° C. to a DMF solution (50 ml) of 2-oxo-1,2-dihydroquinoline-3-carboxaldehyde (5.13 g), followed by stirring for 30 minutes. 4-chlorobenzyl bromide (7.0 g) was added, and the resulting mixture was stirred at room temperature overnight. Water was added to the reaction mixture, extraction with ethyl acetate was performed, and the extract was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:n-hexane=1:10→1:4). The purified product was recrystallized from a chloroform-diisopropyl ether mixed solvent to thereby obtain 6.57 g (yield: 72%) of 1-(4-chlorobenzyl)-2-oxo-1,2-dihydroquinoline-3-carboxaldehyde as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362252B2
Source datasetuspto-grants-2013_01
ORD IDord-6be90d041f454d9197f276171979e49a
Source noteuspto-grants-2013_01