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HRID 1019742作成日:2026年10月25日

Methanol → 1-Chloro-2-fluoro-4-methoxy-5-nitrobenzene

https://huagongshe.com/reaction/1019742

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物WaterHCID 962—
反応物1-Chloro-2,4-difluoro-5-nitrobenzeneHCID 73867—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
生成物1-Chloro-2-fluoro-4-methoxy-5-nitrobenzeneHCID 5340328971%

反応条件

温度0 °C

反応手順

To a mixture of potassium tert-butoxide (3.0 g, 26.9 mmol) in DMF (20 mL), methanol (0.79 g, 24.8 mmol) was added at 0° C. The reaction mixture was stirred at 0° C. for 15 minutes then a solution of 1-chloro-2,4-difluoro-5-nitrobenzene (4.0 g, 20.7 mmol) in DMF (20 mL) was added at 0° C. and the reaction mass stirred for 3 hours at room temperature. Water (200 mL) was added to the reaction mixture and reaction mass was extracted with EtOAc (3×50 mL). The combined organic extracts were washed with water (80 mL), brine (80 mL), dried (Na2SO4) and concentrated under reduced pressure. The product was purified by column chromatography on neutral silica gel using 20-25% EtOAc in hexane to give the desired product (3 g, 71%) as a solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08716287B2
出典データセットuspto-grants-2014_05
ORD IDord-0da0360003694be6aaa3a15d4134a744
出典メモuspto-grants-2014_05