HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 4-Nitroaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Nitrogen oxide (N2O4) | HCID 25352 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Nitroaniline | HCID 7475 | — |
| Product | Diazoaminobenzene | HCID 8689 | — |
| Product | Nitrogen oxide (N2O4) | HCID 25352 | — |
Reaction Steps
Primary aromatic amines also have been diazotized in solvents by means of pure nitrogen tetroxide. O. N. Witt, Tagbl. Natf.-Vers. Baden-Baden 1879, 194 (Chem. Zentr. 1880, II, 226) reported obtaining benzenediazonium nitrate by the reaction of anhydrous pure nitrogen tetroxide with aniline in an anhydrous benzene solution; and B. Houston et al., J. Am. Chem. Soc. 47, 3011-3018 (1925), obtained a diazoaminobenzene derivative as well as the corresponding diazonium nitrate by the action of pure, anhydrous nitrogen tetroxide on o-, m-, and p-nitroaniline in an anhydrous benzene solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04020052 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-368793d34a104beeb6b437a34378f80c |
| Source note | uspto-grants-1977_04 |