HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-bromo-N-tert-butylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Bromobenzenesulfonyl chloride | HCID 520403 | — |
| Product | 2-bromo-N-tert-butylbenzenesulfonamide | HCID 4825014 | 97.1% |
Reaction Steps
2-Bromobenzenesulfonyl chloride (100.9 g, 394.9 mmol) was dissolved in methylene chloride (500 mL, 8.0 mol) and cooled at 0° C. t-Butylamine (41.3 mL, 395 mmol) was added in 3 portions over approximately 1 minute. DIPEA (75.7 mL, 434 mmol) was immediately added in 3 portions over approximately 1 minute. The mixture was warmed to room temperature and stirred overnight. The product was washed with 1M H3PO4 (2×), with saturated. NaHCO3, and with saturated aqueous NaCl, then dried over MgSO4, filtered, and concentrated to yield 2-bromo-N-t-butyl-benzenesulfonamide (112 g) as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822522B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-a7f123144a76456fad9d82b6c413cc94 |
| Source note | uspto-grants-2014_09 |