HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Trifluoromethylcarbonylaminosulphonyl)-3-nitrobenzene → 1-(Trifiuoromethyl carbonylaminosulphonyl)-3-aminobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Trifluoromethylcarbonylaminosulphonyl)-3-nitrobenzene | HCID 18957784 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(Trifiuoromethyl carbonylaminosulphonyl)-3-aminobenzene | HCID 21745506 | 70% |
Reaction Steps
In the same way as that described in Example 11, Step 2, using 1-(trifluoromethylcarbonylaminosulphonyl)-3-nitrobenzene (2.7 g, 9.1 mmol), 10% palladium on carbon (0.25 g, 9% (w/w)) in water (3 ml) and ethanol (70 ml), the title compound (1.7 g, 70%) was afforded as a colourless solid. mp 106°-108° C. 1H NMR (360 MHz, D6 -DMSO) δ 6.59 (1H, m), 6.88 (1H, m), 7.02 (2H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05360802 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-3c6bb15660594b0b8bc84f15131448e1 |
| Source note | uspto-grants-1994_11 |