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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948Generated: October 25, 2026

Nitrobenzene → 5-(N,N-diphenylamino)acenaphthene

https://huagongshe.com/reaction/1948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrobenzeneHCID 7416—
ReactantPotassium CarbonateHCID 11430—
ReactantIodobenzeneHCID 11575—
Reactant5-AminoacenaphtheneHCID 62547—
ReactantN-phenyl-1,2-dihydroacenaphthylen-5-amineHCID 1236299—
CatalystCopperHCID 23978—
SolventTolueneHCID 1140—
Product5-(N,N-diphenylamino)acenaphtheneHCID 1968891975.7%

Reaction Conditions

Temperature200 °C

Reaction Steps

33.85 g (0.2 mol) of 5-aminoacenaphtthene was mixed with 102.1 g (0.5 mol) of iodo benzene, 1.3 g (0.02 mol) of copper powder, 34.5 g (0.25 mol) of anhydrous potassium carbonate and 100 ml of nitrobenzene, and the mixture was stirred at 200° C. for 26 hours. The reaction was determined to be finished when disappearance of 5-aminoacenaphthene and 5-(N-phenylamino)acenaphthene as an intermediate was identified. 300 ml of toluene was added thereto to dissolve a product, and the resultant mixture was filtrated and concentrated. The concentrated product was purified by column chromatography (carrier: silica gel, eluent: toluene/hexane=1/4) to obtain 48.7 g (yield: 75.7%, melting point: 168.5°-170.5° C.) of 5-(N,N-diphenylamino)acenaphthene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728500
Source datasetuspto-grants-1998_03
ORD IDord-34a870e6034145a8adf96361ff614be2
Source noteuspto-grants-1998_03