HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460674Generated: October 29, 2026
1-Iodonaphthalene → HCID 23067344, compound
https://huagongshe.com/reaction/460674
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Iodonaphthalene | HCID 7004 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 23067346 | HCID 23067346 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Mesitylene | HCID 7947 | — |
| Product | HCID 23067344 | HCID 23067344 | 124.6% |
Reaction Steps
2.6 g of 1,3,5-tris(p-tert.-butylphenylamino)benzene, 6.4 g of 1-iodonaphthalene, 6.9 g of potassium carbonate, 1.0 g of copper powder, 0.7 g of 18-crown-6 (or 1,4,7,10,13,16-hexaoxacyclo-octadecane) and 20 mL of mesitylene were placed in a 100 mL capacity flask and the reaction was carried out at a temperature of 170° C. for 16.5 hours under a nitrogen atmosphere. After the reaction, the resultant reaction mixture was extracted with toluene and the toluene solution was subjected to silica gel chromatography to fractionate the reaction product. The reaction product was then purified by recrystallization and then by sublimation to provide 2.8 g of the desired 1,3,5-tris(N-(p-tert.-butylphenyl)-N-(1-naphthyl)amino)-benzene. The yield was 62%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196224B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-6650d9ebaec1423e868ae894e288b150 |
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| Source note | uspto-grants-2007_03 |
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