HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-benzyl-6-chloro-2-hydroxy-3-nitrobenzenesulfonamide → N-Benzyl-3-amino-6-chloro-2-hydroxybenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-benzyl-6-chloro-2-hydroxy-3-nitrobenzenesulfonamide | HCID 18373553 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-Benzyl-3-amino-6-chloro-2-hydroxybenzenesulfonamide | HCID 18373453 | 86.1% |
Reaction Steps
To a solution of N-benzyl-6-chloro-2-hydroxy-3-nitrobenzenesulfonamide (180 mg, 0.52 mmol) in ethyl acetate, was added 10% Pd/C (70 mg). The mixture was flushed with argon, then stirred under a hydrogen atmosphere at balloon pressure for 1 hour at room temperature. The mixture was filtered through celite and the celite was washed with methanol. The solvent was evaporated to give the desired product (140 mg, 85%). 1H NMR (DMSO-d6): δ 8.73 (t, 1H), 7.24 (m, 5H), 6.78 (d, 1H), 4.09 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06500863B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-fbb9a8006a894737831e410b50ad26e0 |
| Source note | uspto-grants-2002_12 |