HRID1780286

反应详情

EQUATION

反应方程式

HRID 1780286 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

0.29 g (6.83 mmol) of sodium hydride (as a 55% w/w dispersion in mineral oil) was added, whilst ice-cooling, to a solution of 1.50 g (4.55 mmol) of ethyl 4-(benzyloxycarbonylamino)phenoxyacetate (prepared as described in Preparation 14) in 9 ml of dimethylformamide, and the mixture was stirred for 20 minutes, after which 0.57 ml (9.10 mmol) of methyl iodide was added to the reaction mixture. The mixture was then stirred at room temperature for 4 hours. At the end of this time, the reaction mixture was neutralized with 1N aqueous hydrochloric acid, and the solvent was removed by distillation under reduced pressure. The resulting residue was mixed with ethyl acetate, and the resulting organic solution was washed with 1N aqueous hydrochloric acid, with a 5% w/v aqueous solution of sodium hydrogencarbonate, with a 5% w/v aqueous solution of sodium thiosulfate and with a saturated aqueous solution of sodium chloride, in that order. The reaction mixture was then dried over anhydrous sodium sulfate, and the solvent was removed by distillation under reduced pressure. The resulting residue was purified by preparative thin layer chromatography, using a 3:2 by volume mixture of hexane and ethyl acetate as the developing solvent, to give 0.69 g of the title compound as an oil.

WORKUP

后处理

  1. stirringThe mixture was then stirred at room temperature for 4 hours
  2. customthe solvent was removed by distillation under reduced pressure
  3. additionThe resulting residue was mixed with ethyl acetate
  4. washthe resulting organic solution was washed with 1N aqueous hydrochloric acid, with a 5% w/v aqueous solution of sodium hydrogencarbonate, with a 5% w/v aqueous solution of sodium thiosulfate and with a saturated aqueous solution of sodium chloride, in that order
  5. dry with materialThe reaction mixture was then dried over anhydrous sodium sulfate
  6. customthe solvent was removed by distillation under reduced pressure
  7. customThe resulting residue was purified by preparative thin layer chromatography
  8. additionby volume mixture of hexane and ethyl acetate as the developing solvent