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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678803Generated: October 25, 2026

Acenaphthenequinone → Acenaphtho[1,2-b]quinoxaline

https://huagongshe.com/reaction/1678803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcenaphthenequinoneHCID 6724—
ReactantO-PhenylenediamineHCID 7243—
SolventWaterHCID 962—
ProductAcenaphtho[1,2-b]quinoxalineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08009267B2
Source datasetuspto-grants-2011_08
ORD IDord-8f3f67ab094c4b6aac28051184d972cd
Source noteuspto-grants-2011_08