反应 #1435730

ord-422d960a922041c29902827a1bcca0d3

反应方程式

Cl
hydrochloric acid
[H-].[Na+]
sodium hydride
CCOC(=O)Cc1c(F)cccc1Cl
ethyl 2-chloro-6-fluorophenylacetate
CC(=O)OC(C)=O
acetic anhydride
CCOC(=O)CC(=O)Cc1c(F)cccc1Cl
ethyl (2-chloro-6-fluorophenyl)acetoacetate
收率 35.8%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwere added dropwise
  2. 2
    温度under reflux
  3. 3
    温度refluxed
  4. 4
    温度under heating for 10 hours
  5. 5
    温度The reaction mixture was cooled
  6. 6
    萃取extracted with t-butyl methyl ether
  7. 7
    洗涤The organic layer was washed with dil. hydrochloric acid, aqueous saturated sodium bicarbonate solution, dil. hydrochloric acid and water
  8. 8
    干燥subsequently, dried over sodium sulfate
  9. 9
    浓缩concentrated

实验过程

Into a mixture of 9.6 g of sodium hydride (60% in oil) and 200 ml of tetrahydrofuran, 21.7 g of ethyl 2-chloro-6-fluorophenylacetate were added dropwise under reflux. Then, a solution of 12.3 g of acetic anhydride in 40 ml tetrahydrofuran was added thereto and refluxed under heating for 10 hours. The reaction mixture was cooled, poured into iced dil. hydrochloric acid and extracted with t-butyl methyl ether. The organic layer was washed with dil. hydrochloric acid, aqueous saturated sodium bicarbonate solution, dil. hydrochloric acid and water, subsequently, dried over sodium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 9.27 g of ethyl (2-chloro-6-fluorophenyl)acetoacetate.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07211545B2uspto-grants-2007_05