HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosuccinimide → 3-(Methylsulfinyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 18461638 | HCID 18461638 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(Methylsulfinyl)benzenesulfonamide | HCID 18461747 | 57% |
Reaction Steps
A mixture of 3-methylsulfanyl-benzenesulfonamide (406 mg, 2 mmol) and N-chlorosuccinimide (268 mg, 2 mmol) in methanol was stirred at room temperature for 8 hours. The methanol was evaporated and the residue was slurried with methylene chloride and filtered. The filtrate was evaporated to give 250 mg of the titled compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06433009B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-8322d8de086c4a9dbac260d0f86ff0e3 |
| Source note | uspto-grants-2002_08 |