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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 917001Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/917001

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt4-IodobiphenylHCID 15322—
Edukt18-Crown-6HCID 28557—
Edukt1,3,5-Tris(l-naphthylamino)benzeneHCID 23139724—
KatalysatorCopperHCID 23978—
LösungsmittelMesityleneHCID 7947—
Produkt1,3,5-Tris(n-(4-biphenylyl)-n-(1-naphthyl)amino)benzeneHCID 23139725110,3%

Reaktionsschritte

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%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07271291B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-8fc0f2e29120456e8994531a6e7e75d7
Quellennotizuspto-grants-2007_09