HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917001Generated: October 26, 2026
Potassium Carbonate → 1,3,5-Tris(n-(4-biphenylyl)-n-(1-naphthyl)amino)benzene
https://huagongshe.com/reaction/917001
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Iodobiphenyl | HCID 15322 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | 1,3,5-Tris(l-naphthylamino)benzene | HCID 23139724 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Mesitylene | HCID 7947 | — |
| Product | 1,3,5-Tris(n-(4-biphenylyl)-n-(1-naphthyl)amino)benzene | HCID 23139725 | 110.3% |
Reaction Steps
2.0 g of 1,3,5-tris(1-naphthylamino)benzene, 5.0 g of 4-iodobiphenyl, 3.7 g of potassium carbonate, 2 g of copper powder, 0.3 g of 18-crown-6 (or 1,4,7,10,13,16-hexaoxacyclooctadecane) and 10 mL of mesitylene as a reaction solvent were placed in a 100 mL capacity glass flask and the reaction was carried out at a temperature of 170° C. for 17 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 from a mixed solvent of toluene/hexane and then by sublimation to provide 1.2 g of the desired 1,3,5-tris(N-(4-biphenylyl)-N-(1-naphthyl)amino)benzene (TBNAB). The yield was 32%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07271291B2 |
|---|
| Source dataset | uspto-grants-2007_09 |
|---|
| ORD ID | ord-8fc0f2e29120456e8994531a6e7e75d7 |
|---|
| Source note | uspto-grants-2007_09 |
|---|