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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506179Generated: October 27, 2026

Iodine → 2-Iodo-5-methyl-4-nitroaniline

https://huagongshe.com/reaction/506179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-Nitro-m-toluidineHCID 11898—
CatalystHCID 178418844HCID 178418844—
Product2-Iodo-5-methyl-4-nitroanilineHCID 58121243—

Reaction Steps

3-Methyl-4-nitroaniline was treated with iodine and silver sulfate to give 2-iodo-5-methyl-4-nitroaniline. Treatment of the nitroaniline with 2-(trimethylsilyl)acetylene under the typical Sonogashira conditions gave 5-methyl-4-nitro-2-[(trimethylsilyl)ethynyl]aniline, which was treated with a base in an aqueous methanolic solution to give 2-ethynyl-5-methyl-4-nitroaniline. A subsequent base-induced cyclization at an elevated temperature gave 5-nitro-6-methylindole, which was treated under a high pressure hydrogenation condition to provide 5-amino-6-methylindole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781591B2
Source datasetuspto-grants-2010_08
ORD IDord-187d4a186cf84ac596d6a843501fc9bd
Source noteuspto-grants-2010_08