HRID245451

反应详情

EQUATION

反应方程式

HRID 245451 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Sodium hydride (0.159 g, 3.97 mmol) was suspended in 20 ml of DMF and cooled in an ice bath. Ethyl 2-(5-((tert-butyldiphenylsilyloxy)methyl)-4-((2R,6S)-2,6-dimethylmorpholino)-2,3-difluorophenyl)-2-(hydroxyimino)acetate (Intermediate 165, 1.94 g, 3.18 mmol) was dissolved in 20 ml of DMF and added to the reaction flask. The ice bath was removed and the reaction stirred at room temperature for 2 hours. The reaction was quenched with sat NH4Cl (5 ml), diluted with water and extracted three times with ethyl acetate. The organic layers were combined, washed with water and brine 5×, dried over MgSO4 and concentrated. The residue was purified by silica gel column chromatography using a gradient of hexanes to ethyl acetate to give the title compound (1.250 g, 66.6%).

WORKUP

后处理

  1. temperaturecooled in an ice bath
  2. additionadded to the reaction flask
  3. customThe ice bath was removed
  4. customThe reaction was quenched with sat NH4Cl (5 ml)
  5. additiondiluted with water
  6. extractionextracted three times with ethyl acetate
  7. washwashed with water and brine 5×
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated
  10. customThe residue was purified by silica gel column chromatography