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 1 l of dioxane is saturated with N2 for 1 h. Then, firstly 0.9 ml (4.3 mmol) of P(tBu)3, then 0.480 g (2.1 mmol) of palladium acetate are added to the solution. 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, 1 l of water is carefully added. The organic phase is washed with 4×50 ml of H2O and dried over MgSO4, and the solvents are removed in vacuo. The pure product is obtained by recrystallisation. The yield is 27 g (64 mmol), corresponding to 76% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09422287B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-875ae68106d94b90860c9c49b6eec3c5 |
| Source note | uspto-grants-2016_08 |