HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Nitro-4-amino-1-naphthol → 5-Nitronaphthalene-1,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Nitro-4-amino-1-naphthol | HCID 21569005 | — |
| Reactant | HCID 178516261 | HCID 178516261 | — |
| Reactant | HCID 178516262 | HCID 178516262 | — |
| Catalyst | Ferrous cation | HCID 27284 | — |
| Product | 5-Nitronaphthalene-1,4-dione | HCID 12336402 | — |
Reaction Steps
5-Nitro-1,4-naphthoquinone is prepared by reducing 8-nitro-1,4-naphthoquinone-1-oxime and/or 5-nitro-1,4-naphthoquinone-1-oxime in an aqueous and/or organic reaction medium in the presence of iron (II) ions and a hydrogen halide at a temperature in the range of from -20° to 100°C, and thereafter oxidizing the 8- and and/or 5-nitro-4-amino-1-naphthol formed, or the corresponding salt, optionally without intermediate isolation, at a temperature in the range of from -10° to 100°C to form the desired 5-nitro-1,4-naphthoquinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03931255 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-0086968c91504490ba5b4f7d4f16714a |
| Source note | uspto-grants-1976_01 |