HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Isopropoxy-N-methyl-3-nitrobenzenesulfonamide → 3-amino-N-methyl-4-[(1-methylethyl)oxy]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Isopropoxy-N-methyl-3-nitrobenzenesulfonamide | HCID 69935238 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-amino-N-methyl-4-[(1-methylethyl)oxy]benzenesulfonamide | HCID 43449295 | 77.6% |
Reaction Steps
To a mixture of N-methyl-4-[(1-methylethyl)oxy]-3-nitrobenzenesulfonamide (1.6 g, 5.8 mmol) in ethanol (20 mL) under nitrogen, Pd/C (0.160 g) was added. The flask was then evacuated and recharged with hydrogen three times. The resulting mixture was allowed to stir under a hydrogen atmosphere overnight at room temperature. The mixture was then filtered and concentrated to afford 3-amino-N-methyl-4-[(1-methylethyl)oxy]benzenesulfonamide (1.1 g, 77%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ 7.01-7.10 (m, 2H), 6.87-6.98 (m, 2H), 5.08 (br. s., 2H), 4.63 (dt, J=5.93, 11.98 Hz, 1H), 2.34-2.41 (m, 3H), 1.29 (d, J=6.02 Hz, 6H); MS (m/z) 244.7 (M+H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859571B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-aa418ae23a0d4180a0fcdf9abd261693 |
| Source note | uspto-grants-2014_10 |