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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507038Generated: November 4, 2026

Iodine chloride → 2-Iodo-4-methyl-5-(trifluoromethyl)aniline

https://huagongshe.com/reaction/507038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodine chlorideHCID 24640—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Methyl-3-(trifluoromethyl)anilineHCID 2737715—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventSodium PyrosulfiteHCID 656671—
Product2-Iodo-4-methyl-5-(trifluoromethyl)anilineHCID 53421146103.1%

Reaction Steps

Add a solution of iodine monochloride (27.8 g, 171 mmol) in dichloromethane (180 mL) to a solution of 4-methyl-3-trifluoromethylaniline (25.0 g, 143 mmol) and sodium bicarbonate (14.4 g, 171 mmol) in methanol (180 mL) and dichloromethane (730 mL) at room temperature under nitrogen. Stir the mixture for 3 h and dilute the cooled mixture with aqueous sodium metabisulfite (500 mL). Collect the organic phase, and extract the aqueous phase with methylene chloride (200 mL). Wash the combined organic extracts with brine (250 mL), dry over anhydrous sodium sulfate and filter. Remove the solvent under reduced pressure to provide a brown oil, which crystallizes upon standing to afford the title compound as brown needles (44.4 g, >99%), which is used in the next step without purification. APCI MS m/z 302 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786108B2
Source datasetuspto-grants-2010_08
ORD IDord-6ef97865e4da4265acbc33d23ec58cbc
Source noteuspto-grants-2010_08