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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066558Generated: October 31, 2026

Water → N-[4-[4-(N-naphthalen-1-ylanilino)phenyl]phenyl]-N-phenylnaphthalen-1-amine

https://huagongshe.com/reaction/1066558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhenyl-1-naphthylamineHCID 7013—
ReactantPotassium CarbonateHCID 11430—
Reactant4,4'-Diiodo-1,1'-biphenylHCID 76348—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
ProductN-[4-[4-(N-naphthalen-1-ylanilino)phenyl]phenyl]-N-phenylnaphthalen-1-amineHCID 506912755.9%

Reaction Conditions

Temperature200 °C

Reaction Steps

To 32.4 g (148 mmol) of N-phenyl-1-naphthylamine were added 25.1 g (61.5 mmol) of 4,4′-diiodobiphenyl, 2.14 g of polyethylene glycol (PEG-6000 (a trade name) manufactured by Wako Junyaku K.K.), 17.1 g (0.124 mol) of potassium carbonate and 15.7 g (247 mmol) of copper (powder) were added, and heated to 200° C. The reaction was traced by high-performance liquid chromatography. Heating was continued under stirring until the peaks of raw materials and intermediates were disappeared (for 12 hours). After the completion of the reaction, water and DMF are added, and the resulting mixture is dispersed, filtrated, and washed with water. The resulting crystal is purified by silica gel chromatography to afford 20.2 g (yield: 55.9%) of N,N′-di(l-naphthyl)-N,N′-diphenyl-4,4′-diaminobiphenyl represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242648B1
Source datasetuspto-grants-2001_06
ORD IDord-29088e5b77284c6194591f130de94947
Source noteuspto-grants-2001_06