HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 605037Erstellt: 25. Oktober 2026
Acenaphthenequinone → Acenaphtho[1,2-b]quinoxaline
https://huagongshe.com/reaction/605037
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acenaphthenequinone | HCID 6724 | — |
| Edukt | O-Phenylenediamine | HCID 7243 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Acenaphtho[1,2-b]quinoxaline | HCID 136028 | — |
Reaktionsschritte
To a reaction vessel equipped with a stirrer, 5-liter of glacial acetic acid and 490 g of purified acenaphthenequinone were added and stirred for 15 minutes under nitrogen bubbling to obtain an acenathphenequinone solution. Similarly, to another reaction vessel equipped with a stirrer, 7.5-liter of glacial acetic acid and 275 g of o-phenylenediamine were added and stirred for 15 minutes under nitrogen bubbling to obtain an o-phenylenediamine solution. Thereafter, while stirring under nitrogen atmosphere, the o-phenylenediamine solution was added to the acenaphthenequinone solution gradually over one hour, and then allowed to react by continuing to stir for 3 hours. After ion exchange water was added to the obtained reaction liquid, the precipitate was filtrated to obtain a crude product. This crude product was recrystallized with a heated glacial acetic acid for purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07911569B2 |
|---|
| Quelldatensatz | uspto-grants-2011_03 |
|---|
| ORD ID | ord-2e7066ef39664a9980ed9e8b283148b5 |
|---|
| Quellennotiz | uspto-grants-2011_03 |
|---|