HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → N-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Iodo-4-nitroaniline | HCID 222629 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-iodo-4-nitrophenyl)-N-(methylsulfonyl)methanesulfonamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871948B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-23c8accabf5148f295a6c4c2ee2b86d0 |
| Source note | uspto-grants-2014_10 |