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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265755Generated: October 28, 2026

1,10-Phenanthroline → 4-Bromo-4',4''-dimethyltriphenylamine

https://huagongshe.com/reaction/265755

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
Reactant4-BromoanilineHCID 7807—
Reactant4-IodotolueneHCID 12207—
ReactantPotassium HydroxideHCID 14797—
SolventO-XyleneHCID 7237—
Product4-Bromo-4',4''-dimethyltriphenylamineHCID 11142701425.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

In a 500 milliliter three-necked flask equipped with a mechanical stirrer, thermometer and Dean-Stark trap, all under an argon atmosphere, were added molten p-iodotoluene (27.3 grams, 125 millimoles), 22 grams of xylene, p-bromoaniline (8.7 grams, 50 millimoles), and 1,10-phenanthroline (1.8 grams, 10 millimoles). The reaction mixture was then heated to 100° C. at which point potassium hydroxide flake (22.4 grams, 400 millimoles) and cuprous chloride (1 gram, 10 millimoles) were added. The temperature was then adjusted to 125° C., and the reaction progress monitored by high performance liquid chromatography. Analysis showed the reaction to be 94 percent complete at 2 hours and 98 percent complete at 5 hours at which point the reaction was terminated. Product isolation was accomplished by adding 24 grams of acetic acid, and partitioning the reaction mixture between 100 grams of toluene and 100 grams of deionized water. The organic phase was further washed several times with deionized water, and the solvent removed to afford 15 grams (84.5 percent) of the desired product of high purity (HPLC, 98 area percent).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05648539
Source datasetuspto-grants-1997_07
ORD IDord-db3f0ecb9ad14ebba93f6d6ea2806266
Source noteuspto-grants-1997_07