Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4,4'-Diiodo-1,1'-biphenyl | HCID 76348 | — |
| Reactant | 4,4'-Di-tert-butyldiphenylamine | HCID 458684 | — |
| Catalyst | Copper | HCID 23978 | — |
| Product | HCID 19708508 | HCID 19708508 | 31.7% |
Reaction Steps
13.4 g (0.048 mol) of 4,4'-ditertiarybutyl-N,N-diphenylamine, 7.7 g (0.019 mol) of 4,4'-diiodobiphenyl, 7.7 g (0.056 mol) of anhydrous potassium carbonate, 0.53 g (0.008 mol) of copper powder, and 5 ml of nitrobenzene were mixed. The reaction mixture was then allowed to undergo reaction at a temperature of 200° to 215° C. for 4 hours. The reaction product was then extracted with 100 ml of THF. The insoluble contents were removed by filtration. The filtrate was then concentrated to obtain a crystal. The crude crystal thus obtained was then purified by column chromatography (carrier: silica gel; elute: 1/2 mixture of toluene and n-hexane) to obtain 4.3 g (yield: 31.7%) of N,N,N',N'-tetrakis(p-tertiarybutylphenyl)benzidine. The melting point of the product was from 402.0° C. to 403.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05707747 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-65c147aea2784dddbd480effef8028c7 |
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| Source note | uspto-grants-1998_01 |
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