HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22622Generated: October 25, 2026
Bromobenzene → N~1~,N~1~,N~5~-Triphenylnaphthalene-1,5-diamine
https://huagongshe.com/reaction/22622
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | 1,5-Diaminonaphthalene | HCID 16720 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | N~1~,N~1~,N~5~-Triphenylnaphthalene-1,5-diamine | HCID 22590762 | 15% |
Reaction Steps
1,5-Diaminonaphthalene (16.0 g, 0.101 mol) was combined with bromobenzene (47.1 g, 0.300 mol), palladium diacetate (1.2 g, 0.004 mol), tri-t-butylphosphine (4 mL), sodium t-butoxide (24.0 g, 0.26 mol), and xylene (400 mL). The mixture was heated at 140° C. with magnetic stirring under a nitrogen atmosphere. After 15 h, an additional amount of palladium diacetate (0.100 g, 0.0004 mol) was added. After heating for another 6 h, an additional amount of palladium diacetate (0.100 g, 0.0004 mol) was added. After heating for another 15 h the heat was removed. After cooling to room temperature, the solid present was filtered off and the filtrate was purified by column chromatography. This afforded 6.0 g (15% yield) of N,N,N′-triphenyl-1,5-diaminonaphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06849345B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-d30650a7d9c94a198aefea829969b8d9 |
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| Source note | uspto-grants-2005_02 |
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