HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11746Erstellt: 24. Oktober 2026
Nitrobenzene → 4,4'-Dibromo-2-bis(4-methoxyphenyl)amino-1,1'-biphenyl
https://huagongshe.com/de/reaction/11746
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Nitrobenzene | HCID 7416 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Iodoanisole | HCID 69676 | — |
| Edukt | 5-Bromo-2-(4-bromophenyl)aniline | HCID 4559420 | — |
| Katalysator | Copper | HCID 23978 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 4,4'-Dibromo-2-bis(4-methoxyphenyl)amino-1,1'-biphenyl | HCID 21976314 | — |
Reaktionsschritte
4,4′-Dibromo-2-amino-1,1′-biphenyl (16.35 g, 0.05 mol), 4-iodoanisole (28 g, 0.12 mol), potassium carbonate (−325 mesh fine powder, 16.6 g, 0.12 mole), copper dust (−150 mesh,1.0 g), and nitrobenzene (20 ml) were charged into a flask and stirred at gentle reflux for 15 hours. The dark reaction mixture was cooled to room temperature and extracted with 200 ml of toluene. The toluene solution was evaporated. The dark residue obtained was then mixed with 10 ml of toluene and chromatographed on a silica gel column using hexane and hexane/ethyl acetate (20:1) eluant. The portions containing the product were collected and evaporated. The residue was recrystallized twice from hexane/toluene (300 ml/60 ml) to yield 7.4 grams of off-white crystals of the desired monomer. 1H NMR (CDCl3): δ=6.8–7.5 (15H, multiple peaks); 3.78 (6H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07098297B2 |
|---|
| Quelldatensatz | uspto-grants-2006_08 |
|---|
| ORD ID | ord-1b201015aa3a453fafae9c0c128bc49f |
|---|
| Quellennotiz | uspto-grants-2006_08 |
|---|