HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Fluoroiodobenzene → 4-Acetyl-4'-fluoro-2-nitrobiphenyl
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Fluoroiodobenzene | HCID 9605 | — |
| Edukt | 1-(4-Bromo-3-nitrophenyl)ethan-1-one | HCID 87737 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-Acetyl-4'-fluoro-2-nitrobiphenyl | HCID 21320555 | — |
Reaktionsschritte
4-fluoroiodobenzene and 4-bromo-3-nitroacetophenone were reacted in an analogous manner to that described in Example 1 (a) to give the novel intermediate 4-acetyl-4'-fluoro-2-nitrobiphenyl, m.p. 88° - 90°C. (from methanol). This compound was reduced with stannous chloride in concentrated hydrochloric acid in an analogous manner to that described in Example 1 (b) to give the novel intermediate 4-acetyl-2-amino-4'-fluorobiphenyl, m.p. 88° - 91°C. (from methanol). The amino group in this compound was converted to methoxy in the following way:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US03969402 |
| Quelldatensatz | uspto-grants-1976_07 |
| ORD ID | ord-fffb69d45e50446d86828345be52bdd9 |
| Quellennotiz | uspto-grants-1976_07 |