反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 55 °C
PROCEDURE
实验过程
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.
WORKUP
后处理
- extractionthe product extracted into CH2Cl2 (5×100 mL)
- washThe organic extracts were washed with water
- dry with materialdried over MgSO4
- customevaporated
- customto give an oily product
- customThe remaining DMF was removed by trituration with petrol
- customThe crude product was purified by flash chromatography (ethyl acetate:petrol 1:1)