反応 #4360

ord-649c77e7ea1f4e54aff363d399cc7db7

反応方程式

CCOC(=O)CC(=O)OCC
diethyl malonate
[Mg]
magnesium
O=C(Cl)c1cc(F)c(Cl)c([N+](=O)[O-])c1Cl
2,4-dichloro-5-fluoro-3-nitro-benzoyl chloride
[H][H]
hydrogen
O=S(=O)(O)O
sulphuric acid
CCOC(=O)C(C(=O)OCC)C(=O)c1cc(F)c(Cl)c([N+](=O)[O-])c1Cl
diethyl (2,4-dichloro-5-fluoro-3-nitro-benzoyl)-malonate
収率 91.0%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONis added dropwise at 50°-60° C
  2. 2
    温度is cooled to -5° to -10° C.
  3. 3
    workup.STIRRINGThereafter, the mixture is stirred at 0° C. for 1 hour
  4. 4
    workup.WAITbrought to room temperature overnight
  5. 5
    温度warmed at 40°-50° C. for a further 2 hours
  6. 6
    workup.ADDITIONis added to the reaction mixture
  7. 7
    温度while cooling with ice
  8. 8
    その他the organic phase is separated off
  9. 9
    抽出The aqueous phase is extracted with toluene
  10. 10
    抽出the combined organic extract
  11. 11
    洗浄is washed with saturated sodium chloride solution
  12. 12
    乾燥dried with sodium sulphate

実験手順

2.1 g of carbon tetrachloride are added to 10.1 g of magnesium filings in 21 ml of ethanol and, when the evolution of hydrogen has started, a mixture of 66.6 g of diethyl malonate, 40 ml of ethanol and 150 ml of toluene is added dropwise at 50°-60° C. The mixture is subsequently stirred at this temperature for 1 hour and is cooled to -5° to -10° C. and a solution of 109.2 g of 2,4-dichloro-5-fluoro-3-nitro-benzoyl chloride in 50 ml of toluene is slowly added dropwise. Thereafter, the mixture is stirred at 0° C. for 1 hour, brought to room temperature overnight and warmed at 40°-50° C. for a further 2 hours. A mixture of 160 ml of water and 10.4 ml of concentrated sulphuric acid is added to the reaction mixture, while cooling with ice, and the organic phase is separated off. The aqueous phase is extracted with toluene, the combined organic extract is washed with saturated sodium chloride solution and dried with sodium sulphate and the solvent is stripped off. 144.5 g of diethyl (2,4-dichloro-5-fluoro-3-nitro-benzoyl)-malonate are obtained as a crude product. This is heated under reflux for 3 hours, after addition of 200 ml of water and 0.6 g of 4-toluenesulphonic acid, and the mixture is extracted with methylene chloride and dried with sodium sulphate and the solvent distilled off in vacuo. 118 g of substituted benzoylacetic acid ester are obtained as a crude product. The product is of sufficient purity for the subsequent reactions.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04725595uspto-grants-1988_02