HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → 2-bromo-N-tert-butyl-4-trifluoromethyl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 2-Bromo-4-(trifluoromethyl)benzenesulfonyl chloride | HCID 2778611 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-bromo-N-tert-butyl-4-trifluoromethyl-benzenesulfonamide | HCID 57934936 | 100% |
Reaction Steps
To a solution of 2-bromo-4-(trifluoromethyl)benzenesulfonyl chloride (10 g, 0.031 mol) in CH2Cl2 (100 mL) was added t-butylamine (8.0 mL, 0.076 mol) at 0° C. The reaction mixture was allowed to warm to room temperature, and stirred for 30 min. A white precipitate formed and was filtered, and the filtrate was concentrated in vacuo to afford the title compound as a yellow oil (11 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612211B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-eb237e66be9a4ee78ea641584e05666b |
| Source note | uspto-grants-2009_11 |