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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226775Generated: November 1, 2026

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

https://huagongshe.com/reaction/2226775

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 mixture of sodium hydroxide (0.4 g.,10 mmol.) in DMSO (20 mL.) was heated to 80°-85° C. for 6 hours to dissolve most of the solids then allowed to cool to room temperature. To the stirred mixture was added 5-bromoindole (2.0 g., 10 mmol.) followed in 1 hour by methyliodide (0.62 mL., 10 mmol.). After stirring for an additional 3 hours the reaction was shown by TLC analysis to be complete. The reaction mixture was diluted with water then extracted with ether. The extracts were washed 2× with water, dried with Na2SO4, and concentrated in vacuo to give 2.08 g. of 1-methyl-5-bromoindole as a yellow oil which crystallized on standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05349061
Source datasetuspto-grants-1994_09
ORD IDord-9cce83c503d045e9a76b419797125c10
Source noteuspto-grants-1994_09