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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739832Generated: November 1, 2026

2-Chloroethyl methyl ether → 6-(4-chlorobenzoyl)-4-(3-chlorophenyl)-1-(2-methoxyethyl)-2(1H)-quinolinone

https://huagongshe.com/reaction/1739832

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl methyl etherHCID 12316—
ReactantSodium hydrideHCID 24758—
Reactant6-(4-chlorobenzoyl)-4-(3-chlorophenyl)-2(1H)-quinolinoneHCID 15524330—
SolventDimethyl SulfoxideHCID 679—
Product6-(4-chlorobenzoyl)-4-(3-chlorophenyl)-1-(2-methoxyethyl)-2(1H)-quinolinoneHCID 2183748236%

Reaction Steps

Sodium hydride (601 g) was added portionwise under N2 flow to a solution of interm. (9-d) (15 g) in dimethyl sulfoxide (200 ml). The mixture was stirred at room temperature for 30 minutes. 2-Chloroethyl methyl ether (25.2 ml) was added. The mixture was stirred at 50° C. for 72 hours, poured out on ice and extracted with ethyl acetate. The organic layer was separated, washed with water, dried (MgSO4), filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: cyclohexane/ethyl acetate 70/30). The pure fractions were collected and the solvent was evaporated, yielding 6.2 g (36%) of 6-(4-chlorobenzoyl)-4-(3-chlorophenyl)-1-(2-methoxyethyl)-2(1H)-quinolinone (interm. 9-e).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968952
Source datasetuspto-grants-1999_10
ORD IDord-a68cd66e68bb448b8df98e3623628a01
Source noteuspto-grants-1999_10