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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628212Generated: October 26, 2026

Potassium Carbonate → 4-(9-Phenyl-9h-carbazol-3-yl)diphenylamine

https://huagongshe.com/reaction/628212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant4-BromodiphenylamineHCID 6425786—
Reactant9-Phenyl-9H-carbazole-3-boronic acidHCID 51358450—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product4-(9-Phenyl-9h-carbazol-3-yl)diphenylamineHCID 5982798345.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a 500 mL three-neck flask were put 6.5 g (26 mmol) of 4-bromodiphenylamine, 7.5 g (26 mmol) of 9-phenyl-9H-carbazole-3-boronic acid, and 400 mg (1.3 mmol) of tri(o-tolyl)phosphine. The atmosphere in the flask was replaced with nitrogen. To the mixture were added 100 mL of toluene, 50 mL of ethanol, and 14 mL (0.2 mol/L) of potassium carbonate aqueous solution. Under reduced pressure, this mixture was degassed while being stirred. After the degassing, 67 mg (30 mmol) of palladium(II) acetate was added to the mixture. This mixture was refluxed at 100° C. for 10 hours. After the reflux, an aqueous layer of this mixture was extracted with toluene, and the extract was combined with an organic layer and then washed with a saturated saline solution. The organic layer was dried with magnesium sulfate. After the drying, this mixture was subjected to gravity filtration. The obtained filtrate was condensed to give an oily light brown substance. This oily substance was purified by silica gel column chromatography (a developing solvent was a mixed solvent of hexane:toluene=4:6). A white solid obtained after the purification was recrystallized with dichloromethane/hexane to give 4.9 g of a white solid, which was the object of the synthesis, in a yield of 45%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09312493B2
Source datasetuspto-grants-2016_04
ORD IDord-601d411158784fa28744c1473b91945d
Source noteuspto-grants-2016_04