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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 238882생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/238882

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Isopropyl iodideHCID 6362—
반응물Cesium carbonateHCID 10796—
반응물4-fluoro-3-hydroxy-N-methoxy-N-methylbenzamideHCID 59459052—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Benzamide,4-fluoro-N-methoxy-N-methyl-3-(1-methylethoxy)-HCID 59459043100%

반응 조건

온도50 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642576B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-f5ebc7c24b174f80a0f49481552bd4ea
출처 메모uspto-grants-2014_02