HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → N-(1,1-Dimethylethyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(1,1-Dimethylethyl)benzenesulfonamide | HCID 314059 | 95.6% |
Reaction Steps
To a cooled (0° C.) solution of tert-butylamine (42.9 mL, 410.6 mmol) in THF (840 mL) was added dropwise benzenesulfonyl chloride (26.2 mL, 205 mmol) and the reaction mixture was stirred at room temperature under an argon atmosphere for 6 h. The mixture was then filtered and the collected solid washed with THF. The filtrate was concentrated, redissolved in CH2Cl2 and washed with 0.1N HCl and H2O. The organic solution was dried and concentrated to afford the desired product (41.8 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05827863 |
| Source dataset | uspto-grants-1998_10 |
| ORD ID | ord-1b6044d52b904ce0a18f29ce5dce3756 |
| Source note | uspto-grants-1998_10 |