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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390119Generated: October 30, 2026

Hydrochloric Acid → 2-Iodo-1-methyl-4-(methylsulfonyl)benzene

https://huagongshe.com/reaction/2390119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
Reactant5-Methanesulfonyl-2-methylanilineHCID 17511954—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product2-Iodo-1-methyl-4-(methylsulfonyl)benzeneHCID 5852206273.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A cooled (0° C.) solution of 2-methyl-5-(methylsulfonyl)aniline (Intermediate 16; 556 mg; 3.00 mmol) in aqueous hydrogen chloride (5 M, 10 mL; 50 mmol) was treated with sodium nitrite (248 mg; 3.60 mmol) and the resulting mixture was stirred at 0° C. for 30 minutes, before being treated with a solution of potassium iodide (4.98 g; 30 mmol) in water (8 mL). The resulting mixture was stirred at RT for 1 hour, the EtOAc was added and the phases separated. The organic layer was washed twice with an aqueous, saturated sodium thiosulfate solution, then with brine, dried over MgSO4 and concentrated to afford a residue which was purified by column chromatography, eluting with cyclohexane containing increasing amounts of EtOAc to afford the title compound (649 mg, 73%) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273769B2
Source datasetuspto-grants-2012_09
ORD IDord-46e2034a46d44cd396422d01d7727824
Source noteuspto-grants-2012_09