HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → 4-bromo-N-tert-butyl-3-methylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | 4-Bromo-3-methylbenzene-1-sulfonyl chloride | HCID 2737503 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-bromo-N-tert-butyl-3-methylbenzenesulfonamide | HCID 7938045 | 89.6% |
Reaction Steps
To a stirred, ice-cold solution of 4-bromo-3-methyl-benzenesulfonyl chloride (11 g, 40.8 mmol) and N′N-diisopropylethylamine (8.5 ml, 49 mmol, 1.2 equiv.) in dichloromethane was added dropwise tert. butylamine (5.2 ml, 49 mmol, 1.2 equiv.). After two hours at room temp., the reaction mixture was diluted with water and extracted with dichloromethane. The organic extracts were concentrated under reduced pressure, the residue stirred with n-heptane and filtered to obtain 11.2 g of the desired compound as a yellow solid. MS (ES): m/e 304.2 (M−H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07868030B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-ae70de4a612a4384b29d889db30582eb |
| Source note | uspto-grants-2011_01 |