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HRID 918129作成日:2026年10月26日

4-Fluoroiodobenzene → 4-Acetyl-4'-fluoro-2-nitrobiphenyl

https://huagongshe.com/reaction/918129

反応式

関与物質

役割名称HCID仕込み量
反応物4-FluoroiodobenzeneHCID 9605—
反応物1-(4-Bromo-3-nitrophenyl)ethan-1-oneHCID 87737—
溶媒MethanolHCID 887—
生成物4-Acetyl-4'-fluoro-2-nitrobiphenylHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US03969402
出典データセットuspto-grants-1976_07
ORD IDord-fffb69d45e50446d86828345be52bdd9
出典メモuspto-grants-1976_07