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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600118Generated: October 25, 2026

Dodecane → N4,N4-di([1,1'-biphenyl]-4-yl)-N4'-phenyl-[1,1'-biphenyl]-4,4'-diamine

https://huagongshe.com/reaction/600118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDodecaneHCID 8182—
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium HydroxideHCID 14797—
ReactantBis-biphenyl-4-yl-amineHCID 504244—
ReactantN-(4'-iodobiphenylyl)acetanilideHCID 23140821—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventIsoamyl AlcoholHCID 31260—
ProductN4,N4-di([1,1'-biphenyl]-4-yl)-N4'-phenyl-[1,1'-biphenyl]-4,4'-diamineHCID 2314081969.9%

Reaction Steps

There were mixed 20.70 g (0.050 mole) of N-(4′-iodobiphenylyl)acetanilide, 19.95 g (0.060 mole) of N,N-bis(biphenyl-4-yl)amine, 10.40 g (0.075 mole) of anhydrous potassium carbonate, 0.20 g (0.003 mole) of copper powder and 10 ml of n-dodecane, followed by reaction at 200 to 212° C. for 15 hours. The reaction product was extracted with 200 ml of toluene, and the insoluble matter was removed by filtration. Then, the filtrate was concentrated to obtain crude crystals. The crude crystals were dissolved in 80 ml of isoamyl alcohol, and 5 ml of water and 5.00 g (0.075 mole) of 85% potassium hydroxide were added, followed by hydrolysis at 130° C. After isoamyl alcohol was removed by steam distillation, extraction with 250 ml of toluene was performed, and the organic layer was washed with water, dried and concentrated. The concentrate was purified by column chromatography (carrier: silica gel, eluate: toluene/n-hexane=1/2) to obtain 24.2 g (yield: 69.9%, HPLC purity: 98.0%) of N,N-bis(biphenyl-4-yl)-N′-phenyl-4,4′-diaminobiphenyl. The melting point was 145.8 to 146.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897816B2
Source datasetuspto-grants-2011_03
ORD IDord-71c0a2f7086e482a881ab9f8dc376607
Source noteuspto-grants-2011_03