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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917001Generated: October 26, 2026

Potassium Carbonate → 1,3,5-Tris(n-(4-biphenylyl)-n-(1-naphthyl)amino)benzene

https://huagongshe.com/reaction/917001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-IodobiphenylHCID 15322—
Reactant18-Crown-6HCID 28557—
Reactant1,3,5-Tris(l-naphthylamino)benzeneHCID 23139724—
CatalystCopperHCID 23978—
SolventMesityleneHCID 7947—
Product1,3,5-Tris(n-(4-biphenylyl)-n-(1-naphthyl)amino)benzeneHCID 23139725110.3%

Reaction Steps

2.0 g of 1,3,5-tris(1-naphthylamino)benzene, 5.0 g of 4-iodobiphenyl, 3.7 g of potassium carbonate, 2 g of copper powder, 0.3 g of 18-crown-6 (or 1,4,7,10,13,16-hexaoxacyclooctadecane) and 10 mL of mesitylene as a reaction solvent were placed in a 100 mL capacity glass flask and the reaction was carried out at a temperature of 170° C. for 17 hours under a nitrogen atmosphere. After the reaction, the resultant reaction mixture was extracted with toluene and the toluene solution was subjected to silica gel chromatography to fractionate the reaction product. The reaction product was then purified by recrystallization from a mixed solvent of toluene/hexane and then by sublimation to provide 1.2 g of the desired 1,3,5-tris(N-(4-biphenylyl)-N-(1-naphthyl)amino)benzene (TBNAB). The yield was 32%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07271291B2
Source datasetuspto-grants-2007_09
ORD IDord-8fc0f2e29120456e8994531a6e7e75d7
Source noteuspto-grants-2007_09