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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277347Generated: October 30, 2026

Nitrogen → Bromo-8-phenyl-8H-8,12b-diazabenzo[a]aceanthrylene

https://huagongshe.com/reaction/2277347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAnilineHCID 6115—
Reactant1,4-DioxaneHCID 31275—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantSodium t-butoxideHCID 23676156—
Reactant3-Bromo-8H-8,12b-diazabenzo[a]aceanthryleneHCID 67325360—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
ProductBromo-8-phenyl-8H-8,12b-diazabenzo[a]aceanthryleneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133119B2
Source datasetuspto-grants-2015_09
ORD IDord-224fd7b4751a4105b0f76b10e7fee648
Source noteuspto-grants-2015_09