HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-Chloro-4-methoxy-1-nitrobenzene → 1-Diethylamino-3-(5'-methoxy-2'-nitro-phenoxy)-naphthalene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-Chloro-4-methoxy-1-nitrobenzene | HCID 593789 | — |
| Edukt | 4-(Diethylamino)naphthalen-2-ol | HCID 15868936 | — |
| Edukt | Oxadiazepine | HCID 21866441 | — |
| Produkt | 1-Diethylamino-3-(5'-methoxy-2'-nitro-phenoxy)-naphthalene | HCID 21438863 | — |
Reaktionsschritte
Thus, for example, a compound of the formula ##STR16## is obtained by reaction of 2-chloro-3-nitro-pyridine with 3-diethylaminothiophenol to give 2(3'-diethylaminothiophenoxy)-3-nitro-pyridine, reduction to the 3-amino compound, diazotisation and intramolecular coupling. The oxadiazepine derivative ##STR17## is obtained, for example, by reaction of 3-chloro-4-nitroanisole with 1-diethylamino-3-hydroxynaphthalene to give 1-diethylamino-3-(5'-methoxy-2'-nitro-phenoxy)-naphthalene, reduction to the 2'-amino compound, diazotisation and internal coupling.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04020063 |
| Quelldatensatz | uspto-grants-1977_04 |
| ORD ID | ord-364b9b4924e84f80b3bd4024e8367219 |
| Quellennotiz | uspto-grants-1977_04 |