HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 4-Nitrosoaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Product | 4-Nitrosoaniline | HCID 69574 | — |
| Product | Nitrous amide, N-phenyl- | HCID 181501 | — |
Reaction Steps
Conventionally, 4-nitrosoaniline is prepared by contacting aniline with sodium nitrite (NaNO2) to produce N-nitrosoaniline and then subjecting the N-nitrosoaniline to Fischer-Hepp rearrangement in acidic condition (Tetrahedron, 1975, 31, 1343-9), or by contacting p-nitrosophenol with ammonia or ammonium chloride (NH4Cl) (U.S. Pat. No. 3,338,966; and J. Chem. Soc., 1955, 2049).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06552229B1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-d6d76e942fdc445ba8a0dff14821f018 |
| Source note | uspto-grants-2003_04 |