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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895570Generated: November 1, 2026

1,4-Cyclohexanedione → 2,3,9,10-Tetrachloro-6,13-pentacenequinone

https://huagongshe.com/reaction/1895570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-CyclohexanedioneHCID 12511—
ReactantPotassium HydroxideHCID 14797—
Reactant1,2-Benzenedicarboxaldehyde, 4,5-dichloro-HCID 9837109—
SolventEthanolHCID 702—
Product2,3,9,10-Tetrachloro-6,13-pentacenequinoneHCID 58289106—

Reaction Steps

4,5-Dichlorobenzene-1,2-dicarbaldehyde (2.0 g, 9.90 mmol) and 1,4-cyclohexanedione (0.62 g, 5.53 mmol) were stirred in 60 mL ethanol. To this was added dropwise with stirring, 10 mL of 5% aq potassium hydroxide. Upon addition of first drop, solution became black, brown, and then solids precipitate. Reaction mixture was stirred at RT for 1 h and refluxed for 2 h. Reaction mixture was cooled to RT, solids filtered, washed with water, dried to give 2,3,9,10-tetrachloro-6,13-pentacenequinone as brown solids in good yields (1.73 g, 70%). LDI-MS m/z: 446 [M+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513466B2
Source datasetuspto-grants-2013_08
ORD IDord-92aef89fec95429ea8495d0caa01b3d6
Source noteuspto-grants-2013_08