HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Nitroaniline → Benzamide, 4-nitro-N-(2-nitrophenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Nitroaniline | HCID 6946 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzamide, 4-nitro-N-(2-nitrophenyl)- | HCID 5155676 | 63.6% |
Reaction Steps
To a mixture of 2-nitroaniline (1.38 g) and triethylamine (1.67 ml) in dichloromethane (30 ml) were added 4-nitrobenzoyl chloride (1.85 g) and the solution was stirred at ambient temperature for 4 hours. The solution was washed successively with 1N hydrochloric acid, saturated aqueous sodium hydrogencarbonate, water and brine, and the organic layer was dried over magnesium sulfate. The solvent was evaporated in vacuo and the residue was solidified with n-hexane to give 2-nitro-N-(4nitrobenzoyl)aniline (1.82 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05521170 |
| Source dataset | uspto-grants-1996_05 |
| ORD ID | ord-884c8b27e2124b9c80f5c99e079dfec6 |
| Source note | uspto-grants-1996_05 |