Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diphenylamine | HCID 11487 | — |
| Reactant | Tricyclohexylphosphine | HCID 75806 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 90458750 | HCID 90458750 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 90460544 | HCID 90460544 | — |
Reaction Steps
A suspension of 9,10-dibromo-1,6,7,12-tetrachloroperylene-3,4-dicarboxylic acid anhidride (1.24 g, 2.0 mmol), diphenylamine (0.40 g, 2.40 mmol), Pd(AcO)2 (10 mmol %), sodium-tert-butoxide (0.48 g, 5.0 mmol), tricyclohexylphosphine (20 mol %) in 70 ml toluene was stirred at 100° C. under argon atmosphere for 24 h. The solvent was removed under reduced pressure. The solid was dissolved in dichloromethane and acetic acid and stirred overnight at 70° C. The solvent was removed under reduced pressure. The crude product was purified by column chromatography using dichloromethane as eluent on silica. Yield 0.50 g (40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428518B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-d0e1522edebc412b9ef4af0bb10ef3ee |
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| Source note | uspto-grants-2016_08 |
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