HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 35990Erstellt: 24. Oktober 2026
4-Aminophenol → 4-(4-Aminophenoxy)-4'-phenylethynylbenzophenone
https://huagongshe.com/de/reaction/35990
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Aminophenol | HCID 403 | — |
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 4-Fluoro-4'-(phenylethynyl)benzophenone | HCID 4095657 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 4-(4-Aminophenoxy)-4'-phenylethynylbenzophenone | HCID 23352813 | 85% |
Reaktionsschritte
In a 250 mL flask equipped with nitrogen inlet, overhead stirring assembly, Dean-Stark trap, and reflux condenser were placed 4-aminophenol (5.46 g, 0.05 mol), 4-phenylethynyl-4'-fluorobenzophenone (15.02 g, 0.05 mol), potassium carbonate (7.6 g, 0.055 mol), toluene (20 mL), and DMAc (45 mL). The mixture was heated to 150° C. for 2 h, then cooled to room temperature. The reaction mixture was poured into water and the resulting light yellow powder was collected by filtration. Recrystallization from toluene afforded the desired product in 85% yield: m.p. 151°-153° C. IR (KBr); 3382 and 3314 cm-1 (NH2); 3049, 1599, and 1509 cm-1 (aromatic C--H); 2217 cm-1 (C=C); and 1645 cm-1 (C=O): Mass Spec. m/e (relative intensity): M+, 389.4 (100); FW=389.44 g/mol.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05412066 |
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| Quelldatensatz | uspto-grants-1995_05 |
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| ORD ID | ord-c9bf34767f6240c1b6e5fc3d71b4a948 |
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| Quellennotiz | uspto-grants-1995_05 |
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