反应 #657306

ord-7cc2b35debf2454a9143f34c10237ba5

反应方程式

[H-].[Na+]
sodium hydride
CC(=O)c1ccc(F)cc1
4-fluoroacetophenone
CCOC(=O)OCC
diethylcarbonate
CCOC(=O)CC(=O)c1ccc(F)cc1
ethyl 3-(4-fluorophenyl)-3-oxopropanoate
收率 83.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Thereafter, the reaction is quenched with aqueous 10% HCl
  2. 2
    萃取extracted with ethyl acetate (2×100 mL)
  3. 3
    干燥The ethyl acetate layer is dried over anhydrous sodium sulphate
  4. 4
    过滤filtered
  5. 5
    浓缩concentrated under reduced pressure
  6. 6
    其他The crude material is purified by column chromatography

实验过程

To a mixture of 4-fluoroacetophenone (20.0 g, 0.145 mol), ethanol (1 mL) and diethylcarbonate (100 mL) is added sodium hydride (60%, 12.0 g, 0.29 mol) at 0° C. portionwise over a period of 30 min. Afterwards the reaction mixture is allowed to warm to room temperature and stirred for 3 h. Thereafter, the reaction is quenched with aqueous 10% HCl and extracted with ethyl acetate (2×100 mL). The ethyl acetate layer is dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure. The crude material is purified by column chromatography using silica gel (230-400 mesh) in ethyl acetate and hexane (1:99 to 5:95) as eluent and 25 g (83%) of ethyl 3-(4-fluorophenyl)-3-oxopropanoate are obtained as light yellow liquid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09023844B2uspto-grants-2015_05