HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877287Generated: October 25, 2026
Di-tert-butylchlorophosphine → 4-(Bis(3-methylphenyl)amino)benz[a]-anthracene
https://huagongshe.com/reaction/877287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Di-tert-butylchlorophosphine | HCID 139566 | — |
| Reactant | Benz(a)anthracene, 4-bromo- | HCID 182324 | — |
| Reactant | m,m'-Ditolylamine | HCID 7016139 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(Bis(3-methylphenyl)amino)benz[a]-anthracene | HCID 59412657 | — |
Reaction Steps
190 μl (1 mmol) of chloro-di-tert-butylphosphine and then 112 mg (0.5 mmol) of palladium(II) acetate are added to a suspension of 15.4 g (50 mmol) of 4-bromobenz[a]anthracene, 11.8 g (60 mmol) of bis(3-methylphenyl)amine and 7.7 g (80 mmol) of sodium tert-butoxide in 500 ml of toluene, and the mixture is subsequently heated under reflux for 5 h. After the mixture has been cooled to 60° C., 500 ml of water are added, the organic phase is separated off, filtered through silica gel, evaporated virtually to dryness at 80° C. in vacuo, and 300 ml of ethanol are then added. After cooling, the solid is filtered off with suction. Recrystallisation five times from dioxane (about 8 ml/g); sublimation (p=5×10−5 mbar, T=280° C.). Yield: 11.9 g (28 mmol), 56.1%, purity 99.9% (HPLC).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08986852B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-b725f01181bc4dc6bc9acb588e93bfa7 |
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| Source note | uspto-grants-2015_03 |
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