HRID841785

反应详情

EQUATION

反应方程式

HRID 841785 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

PROCEDURE

实验过程

To a solution of methyl 3-methoxysalicylate (1.0 g, 5.49 mmol) in 5 ml tetrahydrofuran and 5 ml dimethylformamide was added sequentially at room temperature, benzyl alcohol (0.71 ml, 6.86 mmol), triphenylphosphine (2.16 g, 8.23 mmol) and diethyl azodicarboxylate (1.3 ml, 8.23 mmol). The reaction solution was stirred at room temperature overnight, then ethyl acetate was added and the resulting solution was washed sequentially with water and brine. The ethyl acetate solution was dried over anhydrous sodium sulfate and concentrated to dryness in vacuo. The residue was triturated with diethyl ether and filtered to remove triphenylphosphine oxide. The ether solution was concentrated to dryness in vacuo and the residue was purified by column chromatography on silica gel, eluting with 95:5 hexane/ethyl acetate, yielding the title compound as an oil (870 mg 58% yield). MS (M+1)+273.1

WORKUP

后处理

  1. washthe resulting solution was washed sequentially with water and brine
  2. dry with materialThe ethyl acetate solution was dried over anhydrous sodium sulfate
  3. concentrationconcentrated to dryness in vacuo
  4. customThe residue was triturated with diethyl ether
  5. filtrationfiltered
  6. customto remove triphenylphosphine oxide
  7. concentrationThe ether solution was concentrated to dryness in vacuo
  8. customthe residue was purified by column chromatography on silica gel
  9. washeluting with 95:5 hexane/ethyl acetate