HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → N-t-butyl-3-methyl-4-(trifluoromethanesulfonamido)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | HCID 13194853 | HCID 13194853 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-t-butyl-3-methyl-4-(trifluoromethanesulfonamido)benzenesulfonamide | HCID 13194854 | 34.3% |
Reaction Steps
3-Methyl-4-(trifluoromethanesulfonamido)benzenesulfonyl chloride (1.5 g) was added to tetrahydrofuran (40 ml) containing t-butylamine (0.65 g), and the resultant mixture was allowed to stand at room temperature overnight. The reaction mixture was concentrated and extracted with chloroform. The extract was washed with 5% hydrochloric acid and water in order, dried over anhydrous magnesium sulfate and concentrated. The residue was recrystallized from benzene and then from toluene to give 0.57 g of N-t-butyl-3-methyl-4-(trifluoromethanesulfonamido)benzenesulfonamide (Compound No. 16). M.P., 139.5°-140.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04767446 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-efe5e0d0c4ae41938cfc06ca65b41b15 |
| Source note | uspto-grants-1988_08 |