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HRID 346760作成日:2026年10月26日

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

https://huagongshe.com/reaction/346760

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium hydrideHCID 24758—
反応物2,4-DifluoronitrobenzeneHCID 67967—
反応物N-EthylmethanesulfonamideHCID 5136276—
溶媒DimethylformamideHCID 6228—
生成物N-ethyl-N-(5-fluoro-2-nitrophenyl)methanesulfonamideHCID 22272466—

反応条件

温度55 °C

反応手順

N-ethyl-methanesulfonamide (Mijs et al. J. Chem. Soc. Chem. Com. 1972 p412) (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 % 12.23 H % 4.23; Found N % 10.68 C % 41.39 S % 12.22 H % 4.17.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07173035B2
出典データセットuspto-grants-2007_02
ORD IDord-a4cd6633da1a4f358cd8a1923e7aecb7
出典メモuspto-grants-2007_02