HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(Dimethylaminosulfonyloxy)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Reactant | 2-Hydroxybenzene-1-sulfonamide | HCID 637546 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Dimethylaminosulfonyloxy)benzenesulfonamide | HCID 13473126 | 54.4% |
Reaction Steps
To 6.8 g (0.04 mole) 2-hydroxybenzenesulfonamide in 100 ml methylene chloride was added 4.4 g (0.044 mole) triethylamine and 6.3 g (0.044 mole) dimethylsulfamoyl chloride in 5 ml methylene chloride, keeping the reaction temperature <10° C. The mixture was then warmed to room temperature and stirred 72 hours. The reaction mixture was then diluted with 100 ml methylene chloride washed with 100 ml water, 100 ml 1% HCl and dried over MgSO4. The solvent was evaporated to give a crude yellow oil that slowly solidified on standing. The solids were then triturated with hexanes and filtered to give 6.1 g of a tan solid, m.p. 88°-89° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04515624 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-7a4f7fd8b0564b538ff8cbe360483b86 |
| Source note | uspto-grants-1985_05 |