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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230516생성일: 2026년 10월 25일

Water → N-ethyl-N-(5-fluoro-2-nitrophenyl)methanesulfonamide

https://huagongshe.com/reaction/230516

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium hydrideHCID 24758—
반응물2,4-DifluoronitrobenzeneHCID 67967—
반응물N-EthylmethanesulfonamideHCID 5136276—
용매DimethylformamideHCID 6228—
생성물N-ethyl-N-(5-fluoro-2-nitrophenyl)methanesulfonamideHCID 22272466—

반응 조건

온도55 °C

반응 단계

N-ethyl-methanesulfonamide (Mijs et al. J. Chem. Soc. Chem. Com. 1972 p 412) (5 g 40.6 mmol) was added to a suspension of sodium hydride (1.9 g, 55% in mineral oil) in anhydrous DMF (100 mL) under nitrogen. The mixture was warmed to 55° C. for one hour and 2,4-difluoronitrobenzene (4.4 mL) was added dropwise. The reaction was stirred at 60° C. overnight, poured into water (500 mL) and the product extracted into CH2Cl2 (5×100 mL). The organic extracts were washed with water, dried over MgSO4 and evaporated to give an oily product. The remaining DMF was removed by trituration with petrol. The crude product was purified by flash chromatography (ethyl acetate:petrol 1:1) to yield the desired product which was recrystallised from ethanol. Yield 3.5 g (33%). Calculated N % 10,68 C % 41,22 S % 12,23H % 4,23; Found N % 10,68 C % 41,39 S % 12,22H % 4,17.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566715B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-5ce01ffc76164a8e946b4d6cce206834
출처 메모uspto-grants-2009_07