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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 564833Generated: October 30, 2026

Water → 6-(4-Chlorobenzoyl)-4-(3-methoxyphenyl)-1-methyl-2(1h)-quinolinone

https://huagongshe.com/reaction/564833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
Reactant6-(4-Chlorobenzoyl)-4-(3-methoxyphenyl)-2(1h)-quinolinoneHCID 22714370—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product6-(4-Chlorobenzoyl)-4-(3-methoxyphenyl)-1-methyl-2(1h)-quinolinoneHCID 2271435790%

Reaction Steps

Methyl iodide (1.58 ml) was added to a solution of interm. (5-f) (7.6 g) and benzyl-triethylammonium chloride (BTEAC) (2.23 g) in THF (80 ml) and sodium hydroxide (40%, 80 ml). The mixture was stirred at room temperature for 2 hours. Water was added and the mixture was extracted with ethyl acetate. The organic layer was dried (MgSO4), filtered, and the solvent was evaporated. The residue was purified by flash column chromatography over silica gel (eluent: DCM 100%). The desired fractions were collected and the solvent was evaporated, yielding 7.1 g (90%) of 6-(4-chlorobenzoyl)-4-(3-methoxyphenyl)-1-methyl-2(1H)-quinolinone (interm. 5-g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06169096A
Source datasetuspto-grants-2001_01
ORD IDord-5a7301d618e541988f37bf3bd3aae0b4
Source noteuspto-grants-2001_01