HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → N-(tert-butyl)-2-methoxybenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 2-Methoxybenzenesulfonyl Chloride | HCID 3745851 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(tert-butyl)-2-methoxybenzenesulfonamide | HCID 23448664 | — |
Reaction Steps
A solution of 30.00 g (145.17 mmol) of 2-methoxybenzenesulfonyl chloride in 150 ml of dichloromethane is admixed dropwise at 5-10° C. with 22.30 g (304.87 mmol) of tert-butylamine. The mixture is then stirred at room temperature for 2 h. Following extraction with water, the organic phase is dried over sodium sulfate and evaporated to dryness. This gives 31.10 g (88% of theory) of N-(tert-butyl)-2-methoxybenzenesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855166B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-46014a01d81e47f3aa6d177af405abde |
| Source note | uspto-grants-2010_12 |