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HRID 17736作成日:2026年10月26日

Ethyl Acetate → 4-(4-Chloro-3-ethylphenoxy)-1-nitrobenzene

https://huagongshe.com/reaction/17736

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物p-FluoronitrobenzeneHCID 9590—
反応物Potassium CarbonateHCID 11430—
反応物4-Chloro-3-ethylphenolHCID 84223—
溶媒DimethylformamideHCID 6228—
生成物4-(4-Chloro-3-ethylphenoxy)-1-nitrobenzeneHCID 66977523—

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-chloro-3-ethylphenol (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-(4-chloro-3-ethylphenoxy)-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US07737285B2
出典データセットuspto-grants-2010_06
ORD IDord-c9b591b7bdb2490a88e07295fec5b175
出典メモuspto-grants-2010_06