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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64534Generated: October 29, 2026

9-Acetyl-3-bromocarbazole → N-(9H-carbazol-3-yl)-N-(naphthalen-1-yl)-N',N'-diphenylbenzene-1,4-diamine

https://huagongshe.com/reaction/64534

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-Acetyl-3-bromocarbazoleHCID 1714879—
ReactantN'-1-naphthyl-N,N-diphenyl-1,4-benzenediamineHCID 58811120—
CatalystCopper oxideHCID 14829—
ProductN-(9H-carbazol-3-yl)-N-(naphthalen-1-yl)-N',N'-diphenylbenzene-1,4-diamineHCID 6808896669.6%

Reaction Conditions

Temperature170 °C

Reaction Steps

A mixture of 1.2 g of 9-acetyl-3-bromocarbazole and 2.2 g of N′-1-naphthyl-N,N-diphenyl-1,4-benzenediamine were stirred together in 20 ml N,N′-dimethylacetamide. To this was added 0.8 g of copper oxide and heated to 170° C. for 24 h. The reaction was quenched with water and the solid was filtered, washed with methanol, and dried under vacuum. The solid was then taken up for further deprotection using 0.6 g KOH with TI-IF (3 ml), methanol (6 ml) and water (6 ml) at reflux temperature. The reaction mixture was then extracted using ethyl acetate; and the organic layer was dried over anhydrous sodium sulfate and evaporated to dryness under vacuum. Subsequent silica gel column chromatography using toluene/hexane (½) as eluent, yielded 1.6 g of N-(9H-carbazol-3-yl)-N-(naphthalen-1-yl)-N′,N′-diphenylbenzene-1,4-diamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09450192B2
Source datasetuspto-grants-2016_09
ORD IDord-605fa2acf83047099832614dfeb8157d
Source noteuspto-grants-2016_09