HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64536Generated: October 27, 2026
Benzenamine, 4-methyl-N-(4-methylphenyl)- → 3-(N,N-di-p-tolylamino)-9H-carbazole
https://huagongshe.com/reaction/64536
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenamine, 4-methyl-N-(4-methylphenyl)- | HCID 69293 | — |
| Reactant | 9-Acetyl-3-bromocarbazole | HCID 1714879 | — |
| Catalyst | Copper oxide | HCID 14829 | — |
| Product | 3-(N,N-di-p-tolylamino)-9H-carbazole | HCID 58827521 | 79.5% |
Reaction Steps
A mixture of 1.2 g of 9-acetyl-3-bromocarbazole and 1.2 g of di-p-tolylamine 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 THF (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 1.2 g of 3-(N,N-di-p-tolylamino)-9H-carbazole.
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-d9803ac3404e454084e8800216b6305a |
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| Source note | uspto-grants-2016_09 |
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