HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitrogen → Bromo-8-phenyl-8H-8,12b-diazabenzo[a]aceanthrylene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | 3-Bromo-8H-8,12b-diazabenzo[a]aceanthrylene | HCID 67325360 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Product | Bromo-8-phenyl-8H-8,12b-diazabenzo[a]aceanthrylene | HCID 67325382 | — |
Reaction Steps
A degassed solution of 30 g (86.6 mmol) of 3-bromo-8H-8,12b-diazabenzo[a]aceanthrylene and 8.8 g (95.9 mmol) of phenylamine in 1000 ml dioxane is saturated with N2 for 1 h. Then firstly 0.9 ml (4.3 mmol) of P(tBu)3, then 0.48 g (2.1 mmol) of palladium(II) acetate are added to the solution, and 12.6 g (131 mmol) of NaOtBu in the solid state are subsequently added. The reaction mixture is heated under reflux for 18 h. After cooling to room temperature, 1000 ml of water are carefully added. The organic phase is washed with 4×50 ml of water and dried over MgSO4, and the solvent is removed in vacuo. The pure product is obtained by recrystallisation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133119B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-224fd7b4751a4105b0f76b10e7fee648 |
| Source note | uspto-grants-2015_09 |