HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-tert-butylmethanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-tert-butylmethanesulfonamide | HCID 4130162 | 80.7% |
Reaction Steps
Methanesulfonyl chloride (229 g) was added dropwise to a solution (800 ml) of t-butylamine (420 g) in chloroform under cooling in an ice bath for 90 minutes. After stirring for 3 hours at room temperature, the solution was refluxed under heating for 1 hour. The resulting reaction mixture was cooled with ice, made acidic by adding dilute hydrochloric acid, and extracted with chloroform. The organic layer was washed with water and dried over sodium sulfate. The resulting solution was distilled under reduced pressure to obtain N-t-butylmethanesulfonamide (244 g) as white solid. This product was immediately subjected to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06420409B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-967b9c3b8ec5484ba33933eba8e6f321 |
| Source note | uspto-grants-2002_07 |