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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525148Generated: October 27, 2026

Methyl iodide → 5-Bromo-1-methyl-1H-indole

https://huagongshe.com/reaction/525148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
Reactant5-BromoindoleHCID 24905—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product5-Bromo-1-methyl-1H-indoleHCID 285757—

Reaction Steps

A solution of 5-bromo-1H-indole (1.530 mmol) in dimethyl sulfoxide (10 mL) was treated with NaOH (2.295 mmol) and stirred at room temperature for 30 min. The solution was then treated with methyl iodide (4.59 mmol) and was stirred for 3 days at room temperature. The solution was diluted with water (100 mL) and was extracted with ethyl acetate. The combined organic phases were washed with water, washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The yellow oil was used without further purification. MS(ES)+ m/e 210/212 [M+H]+ (bromide isotope pattern).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09340529B2
Source datasetuspto-grants-2016_05
ORD IDord-02b31b0381b444e3b2920e1314386716
Source noteuspto-grants-2016_05