HRID551899

反应详情

EQUATION

反应方程式

HRID 551899 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 6-({4-[(4-butylphenyl)ethynyl]benzyl}amino)-2,2-dimethyl-4H-1,3-benzodioxin-4-one (150 mg, 0.34 mmol) in anhydrous DCE (3 mL) were added 3-phenylpropionaldehyde (Aldrich, 75 μL, 0.51 mmol) and sodium triacetoxyborohydride (110 mg, 0.51 mmol). The reaction mixture was stirred at rt for 24 hrs. The solvent was removed under reduced pressure. The residue was taken up with an aqueous solution of NaOH (2 mL) and extracted with Et2O (6 ml). The organic layer was dried over Na2SO4 and the solvent was removed under reduced pressure. Purification by flash chromatography on silicagel (pentane/DCM (2/3)) gave 147 mg (77%) of the title compound as a yellow oil. HPLC, Rt: 6.3 min (purity: 99.1%). 1H NMR (CDCl3) δ: 7.45 (m, 4H), 7.32-7.15 (m, 10H), 6.91 (m, 1H), 6.80 (m, 1H), 4.49 (s, 2H), 3.42 (t, J=7.4 Hz, 2H), 2.65 (m, 4H), 1.71 (s, 6H), 1.61 (m, 2H), 1.37 (m, 2H), 0.94 (t, J=7.2 Hz, 3H)

WORKUP

后处理

  1. customThe solvent was removed under reduced pressure
  2. extractionextracted with Et2O (6 ml)
  3. dry with materialThe organic layer was dried over Na2SO4
  4. customthe solvent was removed under reduced pressure
  5. customPurification by flash chromatography on silicagel (pentane/DCM (2/3))