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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 9-Acetyl-3-bromocarbazole | HCID 1714879 | — |
| Reactant | N'-1-naphthyl-N,N-diphenyl-1,4-benzenediamine | HCID 58811120 | — |
| Catalyst | Copper oxide | HCID 14829 | — |
| Product | N-(9H-carbazol-3-yl)-N-(naphthalen-1-yl)-N',N'-diphenylbenzene-1,4-diamine | HCID 68088966 | 69.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09450192B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-605fa2acf83047099832614dfeb8157d |
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| Source note | uspto-grants-2016_09 |
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