Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Quinone | HCID 4650 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1,2-Bis(dibromomethyl)benzene | HCID 83234 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,4-Anthraquinone | HCID 69457 | 47% |
Reaction Steps
In an atmosphere of argon, 60 g (550 mmole) of 1,4-benzoquinone, 100 g (240 mmole) of 1,2-bis(dibromomethyl)benzene and 235 g (1.6 mole) of sodium iodide were dissolved into 850 ml of dry dimethylformamide. After the exothermic reaction was completed, the reaction solution was heated to 70° C. and stirred for 8 hours. After the reaction was completed, the formed crystals were separated by filtration and washed with methanol and water and 23 g (the yield: 47%) of light yellow needle crystals of 1,4-anthraquinone were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06489046B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-8be9bee1de68472bb3c4776a0bed788a |
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| Source note | uspto-grants-2002_12 |
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