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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566031Generated: November 1, 2026

Chloroform → Methyl 6-bromo-2-methylquinoline-3-carboxylate

https://huagongshe.com/reaction/566031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantMethyl acetoacetateHCID 7757—
Reactant4-BromoanilineHCID 7807—
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
SolventDimethylformamideHCID 6228—
ProductMethyl 6-bromo-2-methylquinoline-3-carboxylateHCID 18472460—

Reaction Steps

To DMF (7.18 ml) was dropwise added phosphoryl chloride (8.64 ml) at 0° C., and the mixture was stirred at room temperature for 30 minutes. To the mixture was added methyl acetoacetate (10 ml) at 0° C., and the mixture was stirred at room temperature for 2 hours. The mixture was cooled to 0° C., and to the mixture was added 4-bromoaniline (16.78 g), and the mixture was stirred at 90° C. for 4 hours. To the reaction mixture was added chloroform, and the mixture was neutralized with 8N sodium hydroxide. The organic layer was washed with water and saturated sodium chloride solution, dried with magnesium sulfate and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethyl acetate/hexane=1:2) and was recrystallized from ethyl acetate-hexane to give methyl 6-bromo-2-methylquinoline-3-carboxylate (6.02 g) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-351ccd126c1c46c1997a49c895b542ee
Source noteuspto-grants-2001_01