HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
1,2-Naphthalenedicarboxylic anhydride → Tetrabromonaphthalene-1,2-dicarboxylic acid
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 1,2-Naphthalenedicarboxylic anhydride | HCID 21437 | — |
| Edukt | Bromine | HCID 24408 | — |
| Edukt | Tetrabromonaphthalene-1,2-dicarboxylic anhydride | HCID 53658117 | — |
| Produkt | Tetrabromonaphthalene-1,2-dicarboxylic acid | HCID 19373535 | — |
Reaktionsschritte
Tetrabromonaphthalene-1,2-dicarboxylic anhydride: 2.0 g of naphthalene-1,2-dicarboxylic anhydride, 0.05 g of ferrum reductum and 5.2 ml of bromine are heated at 210° C. for 6 hours using a long intensive condenser. Working up analogously to Example 61a) gives 5.0 g of tetrabromonaphthalene-1,2-dicarboxylic acid, which is converted into the anhydride with acetic anhydride. Yield: 4.8 g (94%), bromine content: 62.4% (theoretical 62.7%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05466805 |
| Quelldatensatz | uspto-grants-1995_11 |
| ORD ID | ord-8825e28c6bd044be90026b65480c3adb |
| Quellennotiz | uspto-grants-1995_11 |