HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrite → N-Nitrosodiphenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrite | HCID 946 | — |
| Reactant | Diphenylamine | HCID 11487 | — |
| Product | N-Nitrosodiphenylamine | HCID 6838 | — |
Reaction Steps
diphenylamine method, where diphenylamine as raw material is nitrosated using a nitrite in an organic solvent to produce N-nitrosodiphenylamine, which is rearranged to 4-nitrosodiphenylamine hydrochloride under the action of anhydrous hydrogen chloride, and then, 4-nitrosodiphenylamine hydrochloride is neutralized with a base to give 4-nitrosodiphenylamine which is finally reduced to 4-aminodiphenylamine by sodium sulfide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084302B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-e70b01ed6e6a4bcc904277bc74d3110e |
| Source note | uspto-grants-2006_08 |