HRID491684

反应详情

EQUATION

反应方程式

HRID 491684 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-benzyloxy-3-chlorobenzaldehyde (4 g, 16.2 mmol) in CH2Cl2 (65 mL), m-CPBA (3.63 g, 77% max, 21.05 mmol) was added and stirred at RT for 5 days. The mixture was washed with a Na2S2O3 solution, then NaHCO3 (sat), and evaporated. The residue was suspended in MeOH (150 mL), NaOMe (0.5 M in MeOH, 60 mL) was added and the mixture was stirred for 1 h. The mixture was concentrated, and the residue was dissolved in water, and extracted with Et2O/EtOAc. The aqueous layer was acidified, and extracted with EtOAc. The combined organic portions were dried with Na2SO4, filtered and evaporated. The mixture was purified by column chromatography using CH2Cl2 as the eluent to yield an off-white solid. MS(MH+)=NA; Calc'd 361.09 for C22H16ClNO2.

WORKUP

后处理

  1. washThe mixture was washed with a Na2S2O3 solution
  2. customNaHCO3 (sat), and evaporated
  3. additionNaOMe (0.5 M in MeOH, 60 mL) was added
  4. stirringthe mixture was stirred for 1 h
  5. concentrationThe mixture was concentrated
  6. dissolutionthe residue was dissolved in water
  7. extractionextracted with Et2O/EtOAc
  8. extractionextracted with EtOAc
  9. dry with materialThe combined organic portions were dried with Na2SO4
  10. filtrationfiltered
  11. customevaporated
  12. customThe mixture was purified by column chromatography
  13. customto yield an off-white solid