反応 #4360
ord-649c77e7ea1f4e54aff363d399cc7db7
反応方程式
反応条件
後処理
- 1workup.ADDITIONis added dropwise at 50°-60° C
- 2温度is cooled to -5° to -10° C.
- 3workup.STIRRINGThereafter, the mixture is stirred at 0° C. for 1 hour
- 4workup.WAITbrought to room temperature overnight
- 5温度warmed at 40°-50° C. for a further 2 hours
- 6workup.ADDITIONis added to the reaction mixture
- 7温度while cooling with ice
- 8その他the organic phase is separated off
- 9抽出The aqueous phase is extracted with toluene
- 10抽出the combined organic extract
- 11洗浄is washed with saturated sodium chloride solution
- 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.