HRID1520183

反应详情

EQUATION

反应方程式

HRID 1520183 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

To a solution of 7-fluoro-1,2,3,4-tetrahydroquinolin-2-one (1.5 g, 9.08 mmol) in tetrahydrofuran (50 ml) was dropwise BH3 in THF (1M, 90 ml), the solution was stirred for 24 h at 60° C. The reaction mixture was cooled and then quenched by the addition of methanol (15 ml) and HCl (conc) (5 ml), then stirred for 1 h at 60° C. The reaction mixture was cooled to room temperature and adjusted to pH 12 with sodium hydroxide (4 mol/L), extracted with (3×15 ml) of ethyl acetate and the organic layers were combined and dried over anhydrous magnesium sulfate, concentrated in vacuo to give a residue, which was purified by a silica gel column chromatography with 3% ethyl acetate in petroleum ether to afford 7-fluoro-1,2,3,4-tetrahydroquinoline as a yellow solid (0.9 g, 66%).

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled
  2. customquenched by the addition of methanol (15 ml) and HCl (conc) (5 ml)
  3. stirringstirred for 1 h at 60° C
  4. temperatureThe reaction mixture was cooled to room temperature
  5. extractionextracted with (3×15 ml) of ethyl acetate
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customto give a residue, which
  9. customwas purified by a silica gel column chromatography with 3% ethyl acetate in petroleum ether