Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 4-Hydroxybiphenyl | HCID 7103 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 23089721 | HCID 23089721 | — |
Reaction Steps
Under a nitrogen atmosphere, 4.3 parts of 4-phenylphenol and 1.5 parts of potassium hydroxide were dissolved in 80 parts of toluene and the solution was refluxed under heat. After stirred for 5 hours, the solution was allowed to cool, and the precipitated solid was filtered. Then, under a nitrogen stream, the precipitate, 2 parts of 1,5-dichloroanthraquinone and 0.6 part of copper powder were dissolved in 10 parts of DMF, and the mixture was refluxed under heat for 3 hours. The reaction solution was poured into an aqueous potassiumhydroxide solution, and the precipitated solid was filtered, washed, and dried. Then, after removal of inorganic materials with toluene, the solid obtained was recrystallized from 2-ethoxyethanol, filtered, washed, and dried, to give 0.6 part of 1,5-bis(4-phenylphenoxy)anthraquinone as an intermediate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07494721B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-9b8d4a0ecddf4f1aa2cc428963ba0ff0 |
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| Source note | uspto-grants-2009_02 |
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