HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605037Generated: October 25, 2026
Acenaphthenequinone → Acenaphtho[1,2-b]quinoxaline
https://huagongshe.com/reaction/605037
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acenaphthenequinone | HCID 6724 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Solvent | Water | HCID 962 | — |
| Product | Acenaphtho[1,2-b]quinoxaline | HCID 136028 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07911569B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-2e7066ef39664a9980ed9e8b283148b5 |
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| Source note | uspto-grants-2011_03 |
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