HRID247786

反应详情

EQUATION

反应方程式

HRID 247786 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of 4-benzyloxybenzoic acid chloride (4.3 g) in methylene chloride (50 ml) was slowly added under ice cooling a solution of optically active 1,1,1-trifluoro-2-octanol (2.9 g), dimethylaminopyridine (0.6 g) and triethylamine (1.7 g) in methylene chloride (50 ml). The mixture was left to stand until it reached room temperature and allowed to react overnight. The mixture was poured in ice water and extracted with methylene chloride. The extracted layer was washed with dilute aqueous hydrochloric acid solution, water, 1N aqueous sodium carbonate solution and water, in this order, and dried over anhydrous magesium sulfate. After the solution was distilled to remove the solvent, the crude product obtained was purified by silica-gel column chromatography and recrystallized from ethanol to obtain the titled compound (3.8 g).

WORKUP

后处理

  1. waitThe mixture was left
  2. customreached room temperature
  3. customto react overnight
  4. extractionextracted with methylene chloride
  5. washThe extracted layer was washed with dilute aqueous hydrochloric acid solution, water, 1N aqueous sodium carbonate solution and water, in this order
  6. dry with materialdried over anhydrous magesium sulfate
  7. distillationAfter the solution was distilled
  8. customto remove the solvent
  9. customthe crude product obtained
  10. customwas purified by silica-gel column chromatography
  11. customrecrystallized from ethanol