HRID29881
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
PROCEDURE
实验过程
Alternatively, 3-(4-fluoro-phenoxy)-phenylamine was prepared by a two-step procedure by heating a suspension of m-fluoronitrobenzene (4.06 g, 28.7 mmol), p-fluorophenol (3.21 g, 28.6 mmol) and K2CO3 (8.13 g, 58.8 mmol) in DMA (dimethylamine) (60 mL) at 150° C. for 3 hours. The brown reaction mixture was concentrated to one-quarter original volume, diluted with ethyl acetate (220 mL) and washed successively with water (220 mL), 1N NaOH (220 mL) and brine (220 mL). The organic layer was dried (MgSO4) and the solvent removed in vacuo to afford the diphenylether (5.30 g, 80%) as a brown oil.
WORKUP
后处理
- customAlternatively, 3-(4-fluoro-phenoxy)-phenylamine was prepared by a two-step procedure
- temperatureby heating
- concentrationThe brown reaction mixture was concentrated to one-quarter original volume
- additiondiluted with ethyl acetate (220 mL)
- washwashed successively with water (220 mL), 1N NaOH (220 mL) and brine (220 mL)
- dry with materialThe organic layer was dried (MgSO4)
- customthe solvent removed in vacuo