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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403456Generated: November 2, 2026

2-Methylindole → 5-Bromo-2-methylindole

https://huagongshe.com/reaction/1403456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylindoleHCID 7224—
ReactantBromineHCID 24408—
CatalystSilver sulfateHCID 159865—
SolventSulfuric AcidHCID 1118—
Product5-Bromo-2-methylindoleHCID 500396875%

Reaction Steps

To a solution of 2-methyl-1H-indole (5.0 g, 38.12 mmol) in sulfuric acid (80 mL) was added Ag2SO4 (12.5 g, 40.06 mmol) with ice cooling, and the solution was stirred for 30 min. Then Br2 (6.4 g, 40.05 mmol) was added to the solution dropwise over 30 min. After the solution was stirred for 4 h at room temperature, the reaction was then quenched by the addition of water/ice (300 mL). The reaction mixture was extracted with dichloromethane (3×200 mL) and the organic layers combined, dried over anhydrous sodium sulfate and concentrated in vacuo to afford 5-bromo-2-methyl-1H-indole as a light brown solid (6 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-099afcc770cf41f6a59edca7acb97aee
Source noteuspto-grants-2014_12