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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947435Generated: October 30, 2026

Ammonium Chloride → N-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamide

https://huagongshe.com/reaction/1947435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Iodo-4-nitroanilineHCID 222629—
SolventDichloromethaneHCID 6344—
ProductN-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamideHCID 67284344—

Reaction Steps

To a solution of 2-iodo-4-nitroaniline (1.02 g, 3.86 mmol) in dichloromethane (10 ml), has been added under stirring triethylamine (1.77 ml, 12.7 mmol). To this mixture, a solution of methanesulphonyl chloride (0.98 ml, 12.7 mmol) in dichloromethane (2 ml) has been added dropwise, very slowly and in an ice-bath. The mixture so obtained was left under stirring at room temperature overnight. The day after, the reaction mixture was neutralized with a saturated aqueous solution of NH4Cl. The organic phase was separated, and, after evaporation of the solvent, the residue has been washed with ethanol and filtered to give N-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)-methanesulfonamide as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399477B2
Source datasetuspto-grants-2013_03
ORD IDord-58c8e0970a61404b8d55bc347df337aa
Source noteuspto-grants-2013_03