HRID1106797

反应详情

EQUATION

反应方程式

HRID 1106797 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

5-Bromo-2-(phenethyl)benzaldehyde (1.27 g) and methyl 4-aminobenzoate (0.66 g) were heated together at 110° C. for 30 minutes and for a further 30 minutes under vacuum. The mixture was dissolved in toluene, evaporated to dryness, dissolved in ethanol (15 ml). Sodium borohydride (0.33 g) was added, the mixture stirred for 18 hours, the solvent evaporated and the residue mixed with acetic acid and partitioned between saturated aqueous sodium hydrogen carbonate and ethyl acetate. The organic layer was washed with brine, dried (MgSO4), filtered and evaporated. The resulting residue was purified by MPLC, eluting with dichloromethane, to give methyl 4-[N-(5-bromo-2-(phenethyl)benzyl)amino]benzoate (1.65 g).

WORKUP

后处理

  1. customevaporated to dryness
  2. dissolutiondissolved in ethanol (15 ml)
  3. additionSodium borohydride (0.33 g) was added
  4. customthe solvent evaporated
  5. additionthe residue mixed with acetic acid
  6. custompartitioned between saturated aqueous sodium hydrogen carbonate and ethyl acetate
  7. washThe organic layer was washed with brine
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. customevaporated
  11. customThe resulting residue was purified by MPLC
  12. washeluting with dichloromethane