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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953Generated: October 25, 2026

Nitrobenzene → 5-[N-(4-tolyl)-N-phenylamino]acenaphthene

https://huagongshe.com/reaction/1953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrobenzeneHCID 7416—
ReactantPotassium CarbonateHCID 11430—
ReactantIodobenzeneHCID 11575—
Reactant5-[N-(4-tolyl)amino]acenaphtheneHCID 19688914—
CatalystCopperHCID 23978—
SolventTolueneHCID 1140—
Product5-[N-(4-tolyl)-N-phenylamino]acenaphtheneHCID 1968891383.8%

Reaction Steps

4.66 g (0.018 mol) of the above prepared 5-[N-(4-tolyl)amino]acenaphthene was mixed with 4.99 g (0.022 mol) of iodo benzene, 0.13 g (0.002 mol) of copper powder, 2.76 g (0.02 mol) of anhydrous potassium carbonate and 5 ml of nitrobenzene, and the resultant mixture was stirred at 200° C. for 25 hours. The reaction was determined to be finished when disappearance of 5-[N-(4-tolyl)amino]acenaphthene was identified. 100 ml of toluene was added thereto to dissolve the reaction product, and the mixture was filtrated and concentrated. The concentrated material thus obtained was purified by column chromatography (carrier: silica gel, eluent: toluene/hexane=1/4) to obtain 5.06 g (yield: 83.8%, melting point: 147.0°-148.0° C.) of 5-[N-(4-tolyl)-N-phenylamino]acenaphthene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728500
Source datasetuspto-grants-1998_03
ORD IDord-a22b523213134b988e3fb268968dfa76
Source noteuspto-grants-1998_03