HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-nitro-N-(phenylsulfonyl)Benzamide → 3-Amino-N-(phenylsulfonyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-nitro-N-(phenylsulfonyl)Benzamide | HCID 975733 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Amino-N-(phenylsulfonyl)benzamide | HCID 18405500 | 67.9% |
Reaction Steps
In the same way as that described in Example 11, Step 2, using 1-(phenylsulphonylaminocarbonyl)-3-nitrobenzene (5 g, 16 mmol), 10% palladium on carbon (0.5 g, 10% (w/w)) in water (3 ml) and ethanol (100 ml), the title compound (3 g,67%) was afforded as a pale beige solid after recrystallisation from ethanol. mp 135°-138° C. 1H NMR (360 MHz, D6 -DMSO) δ 6.75-6.78 (1H, m), 6.96-6.98 (2H, m), 7.10 (1H, dd, J=8.0 and 8.0 Hz), 7.60-7.73 (3H, m), 7.97 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05360802 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-8768efc08474453587935b8e1019de6f |
| Source note | uspto-grants-1994_11 |