HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butylamine → methyl 2-(N-tert-butylsulfamoyl)-4-nitrobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butylamine | HCID 6385 | — |
| Reactant | Methyl 2-(chlorosulfonyl)-4-nitrobenzoate | HCID 15240541 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl 2-(N-tert-butylsulfamoyl)-4-nitrobenzoate | HCID 15240542 | — |
Reaction Steps
206 g of tert-butylamine are added dropwise to a solution of 384 g of methyl 2-chlorosulfonyl-4-nitro-benzoate (Example b) in 1500 ml of ethyl acetate at 0° C. The reaction mixture is then allowed to warm up to room temperature and is stirred at this temperature for 1 hour. After washing with dilute hydrochloric acid and water, the organic phase is dried over MgSO4 and concentrated. The residue is extracted by stirring with diisopropyl ether; Yield of sulfonamide: 377.6 g; m.p.: 122-124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06498253B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-fa067522dd3944488487a7fb25541f81 |
| Source note | uspto-grants-2002_12 |