HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Hydroxy-2-nitrobenzoic acid → 4,4'-Diaminodiphenyl Ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Hydroxy-2-nitrobenzoic acid | HCID 11882 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-5-nitrobenzoic acid | HCID 17287 | — |
| Reactant | 3-Chloro-2-nitrobenzoic acid | HCID 20902 | — |
| Reactant | 2-Hydroxy-5-nitrobenzenesulfonic acid | HCID 69225 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Product | 4,4'-Diaminodiphenyl Ether | HCID 7579 | — |
Reaction Steps
A 5-hydroxy-2-nitrobenzoic acid derivative (e.g. sodium 5-hydroxy-2-nitrobenzoate) or a 2-hydroxy-5-nitrobenzenesulfonic acid derivative (e.g. sodium 2-hydroxy-5-nitrobenzoate) is reacted with a 5 chloro-2-nitrobenzoic acid derivative or a 2-chloro-5-nitrobenzoic acid derivative in the presence of an alkali (e.g. sodium hydroxide), followed by hydrogenation using palladium-carbon, to give the corresponding 4,4′-diaminodiphenyl ether derivative. This is diazotized using sodium nitrite under acidic conditions in the presence of hydrochloric acid, followed by reaction with sodium azide, to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06908719B1 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-0abdd3727e3f49e2a53f45e13683e264 |
| Source note | uspto-grants-2005_06 |