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HRID 901721作成日:2026年10月23日

4-Bromophenol → 1-(4-Bromophenoxy)-2-nitrobenzene

https://huagongshe.com/ja/reaction/901721

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromophenolHCID 7808—
反応物Ethyl AcetateHCID 8857—
反応物p-FluoronitrobenzeneHCID 9590—
反応物Potassium CarbonateHCID 11430—
溶媒DimethylformamideHCID 6228—
生成物1-(4-Bromophenoxy)-2-nitrobenzeneHCID 254261—

反応条件

温度80 °C

反応手順

To a stirred solution of 1-fluoro-4-nitrobenzene (10 mmol) in DMF (20 mL) at rt, solid potassium carbonate (30 mmol) was added followed by addition of 4-bromophenol (10 mmol) to the reaction mixture and heating to 80° C. until the reaction was complete as indicated by TLC or HPLC. After cooling to rt, the reaction mixture was poured into EtOAc (100 mL), washed with H2O (2×50 mL) and brine (50 mL), and dried over sodium sulfate. The solvent was removed in vacuuo to afford the desired 4-bromophenoxy-1-nitrobenzene. The crude product was used for further transformation.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07361678B2
出典データセットuspto-grants-2008_04
ORD IDord-3064036248c64e758316fd686d64b966
出典メモuspto-grants-2008_04