HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Acetyl-4-aminobiphenyl → Acetamide, N-(3-nitro(1,1'-biphenyl)-4-yl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Acetyl-4-aminobiphenyl | HCID 19998 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Acetamide, N-(3-nitro(1,1'-biphenyl)-4-yl)- | HCID 79364 | 42.1% |
Reaction Steps
4-Acetaminobiphenyl (17 g, 80.57 mmol)in glacial acetic acid (600 ml) was added a solution of potassium nitrate (18 g, 178 mmol) in conc. sulphuric acid (75 ml) at such a rate that the temperature was kept below 30° C. Following the addition the mixture was stirred at ambient temperature for 72 hours. The reaction mixture was poured into ice-water (1200 ml). The product was filtered off, washed thoroughly with water and dried. Recrystallization from EtOH (99%, 150 ml) afforded 4-acetamino-3-nitrobiphenyl (8.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554630 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-ef4eecd944054dbb9b866479b57c88ed |
| Source note | uspto-grants-1996_09 |