化工社化工社 化学情報印刷レポート · 研究参考用
4-Fluoroiodobenzene → 4-Acetyl-4'-fluoro-2-nitrobiphenyl
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Fluoroiodobenzene | HCID 9605 | — |
| 反応物 | 1-(4-Bromo-3-nitrophenyl)ethan-1-one | HCID 87737 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 4-Acetyl-4'-fluoro-2-nitrobiphenyl | HCID 21320555 | — |
反応手順
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:
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US03969402 |
| 出典データセット | uspto-grants-1976_07 |
| ORD ID | ord-fffb69d45e50446d86828345be52bdd9 |
| 出典メモ | uspto-grants-1976_07 |