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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454285Generated: October 30, 2026

Quinoline → 4-bromo-5-methoxy-1H-indole

https://huagongshe.com/reaction/454285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinolineHCID 7047—
Reactant4-Bromo-5-methoxy-1H-indole-2-carboxylic acidHCID 13356515—
CatalystHCID 178505374HCID 178505374—
Product4-bromo-5-methoxy-1H-indoleHCID 2203055867%

Reaction Conditions

Temperature245 °C

Reaction Steps

4-Bromo-5-methoxyindole-2-carboxylic acid (1.25 g, 4.19 mmol), quinoline (15 ml) and copper chromite (313 mg) were mixed together. Nitrogen was gently bubbled through the mixture for 5 minutes, then the mixture heated quickly to 245° C. under an atmosphere of nitrogen. After 90 minutes the mixture was cooled to ambient temperature diluted with ethyl acetate (100 ml) and washed with 2M aqueous hydrochloric acid (60 ml). The ethyl acetate layer was filtered, the filtrate dried (MgSO4) and the solvent evaporated. The residue was purified by silica column chromatography eluting with dichloromethane/hexane (1/1) to give 4-bromo-5-methoxyindole (635 mg, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-0fdf936fdda14e459420b187dfba4f1b
Source noteuspto-grants-2013_07