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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387960Generated: November 1, 2026

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

https://huagongshe.com/reaction/1387960

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 numberUS06268354B1
Source datasetuspto-grants-2001_07
ORD IDord-986548c9a9594798a4856010c27a3ef4
Source noteuspto-grants-2001_07