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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485589Generated: October 30, 2026

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

https://huagongshe.com/reaction/1485589

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 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422287B2
Source datasetuspto-grants-2016_08
ORD IDord-875ae68106d94b90860c9c49b6eec3c5
Source noteuspto-grants-2016_08