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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236063Generated: October 25, 2026

1,10-Phenanthroline → 4,4'-Dibromotriphenylamine

https://huagongshe.com/reaction/2236063

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantIodobenzeneHCID 11575—
ReactantPotassium HydroxideHCID 14797—
ReactantBis(4-bromophenyl)amineHCID 629950—
CatalystCuprous chlorideHCID 62652—
SolventTolueneHCID 1140—
Product4,4'-DibromotriphenylamineHCID 13594707—

Reaction Conditions

Temperature130 °C

Reaction Steps

In an oxygen-free glovebox, a 250 mL flask was charged with 4,4′-dibromodiphenylamine (15.0 g, 45.8 mmol), iodobenzene (18.7 g, 91.7 mmol), 1,10-phenanthroline (0.827 g, 4.59 mmol), CuCl (0.454 g, 4.59 mmol), KOH (15.4 g, 275 mmol), and toluene (125 mL). The flask was sealed and removed from the glovebox and heated to 130° C. and stirred for 24 hr. The flask was then removed from the oil bath and allowed to cool to room temperature. The solids were filtered off and the solvent was removed to yield a bluish oily substance, which was passed through silica gel column using toluene as the eluant. The fractions were collected and the solvent was removed followed by vacuum distillation at 160° C. for 30 min to remove the remaining iodobenzene to afford a blue solid. This solid was further purified by a second silica plug column using hexanes as the eluant. The colorless clear fractions were combined and the solvent removed to yield the desired product. Purity: 99+%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714099B2
Source datasetuspto-grants-2010_05
ORD IDord-3c668fb43c824d969da6183007a60f23
Source noteuspto-grants-2010_05