HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Cyclohexanedione → 2,3,9,10-Tetrachloro-6,13-pentacenequinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Cyclohexanedione | HCID 12511 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,2-Benzenedicarboxaldehyde, 4,5-dichloro- | HCID 9837109 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2,3,9,10-Tetrachloro-6,13-pentacenequinone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513466B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-92aef89fec95429ea8495d0caa01b3d6 |
| Source note | uspto-grants-2013_08 |