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HRID 238882作成日:2026年10月25日

Dimethylformamide → Benzamide,4-fluoro-N-methoxy-N-methyl-3-(1-methylethoxy)-

https://huagongshe.com/reaction/238882

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Isopropyl iodideHCID 6362—
反応物Cesium carbonateHCID 10796—
反応物4-fluoro-3-hydroxy-N-methoxy-N-methylbenzamideHCID 59459052—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Benzamide,4-fluoro-N-methoxy-N-methyl-3-(1-methylethoxy)-HCID 59459043100%

反応条件

温度50 °C

反応手順

A 2 L round bottom flask equipped with a mechanical stirrer, a N2 inlet, a condenser and a temperature controller, was charged 4-fluoro-3-hydroxy-N-methoxy-N-methylbenzamide (99.6 g, 0.5 mol), isopropyl iodide (110.5 g, 0.65 mol) and Cs2CO3 (195.5 g) and DMF (300 mL). The reaction mixture was heated at 50° C. for 3 h. Isopropyl iodide (17.0 g, 0.1 mol) was added and the reaction was heated at 50° C. for 12 h. The reaction mixture was allowed to cool to rt and water (1 L) and CH2Cl2 (500 mL) were added. The reaction mixture was stirred at rt for 0.5 h, and the organic phase was separated. The aqueous layer was extracted with CH2Cl2 (3×500 mL). The combined organic extracts were washed with water (2×1 L), brine (1 L), dried over MgSO4, filtered and concentrated in vacuo at 40° C. for 18 h to give 4-fluoro-3-isopropoxy-N-methoxy-N-methlbenzamide as an off-white solid (120.0 g, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642576B2
出典データセットuspto-grants-2014_02
ORD IDord-f5ebc7c24b174f80a0f49481552bd4ea
出典メモuspto-grants-2014_02