Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | p-Toluenesulfonanilide, 4'-fluoro- | HCID 853960 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 18509257 | HCID 18509257 | 97% |
Reaction Steps
To a suspension of 4′-fluoro-p-toluenesulfonanilide (486.6 g (1.80 mol) in acetic acid (955 ml), 97% fuming nitric acid (128.6 g (1.98 mol) was added dropwise, keeping the inner temperature at 45° C., over a period of 40 minutes. After completion of the addition, the reaction mixture was stirred at 50° C. for 2 hours and left to cool to room temperature. Water (2000 ml) was then added and the mixture was stirred for 30 minutes. The crystals separated were filtered and washed with water to give 543.5 g (97%) of 4′-fluoro-2′-nitro-p-toluenesulfonanilide as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06586617B1 |
|---|
| Source dataset | uspto-grants-2003_07 |
|---|
| ORD ID | ord-13e55f2a2391422388b940b3966c10d5 |
|---|
| Source note | uspto-grants-2003_07 |
|---|