HRID2054897

反应详情

EQUATION

反应方程式

HRID 2054897 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

To a solution of 0.200 g (0.839 mmol) of the above benzonitrile in EtOH (2 mL), cooled to 0° C., was added 1.0 mL (3.1 mmol) of sodium ethoxide. The reaction was heated to 70° C. for 15 h then cooled to room temperature and an additional 1.0 mL (3.1 mmol) of sodium ethoxide was added. The mixture was heated to 70° C. for an additional 15 h. The reaction was cooled to room temperature and excess base was consumed by the addition of a saturated aqueous solution of NH4Cl. The mixture was diluted with H2O and washed with CH2Cl2. The combined organic phase was dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by flash silica gel chromatography to provide after 0.048 g (21%) of 2-ethoxy-6-fluoro-4-(4-hydroxy-piperidin-1-yl)-benzonitrile as a white solid.

WORKUP

后处理

  1. temperaturethen cooled to room temperature
  2. temperatureThe mixture was heated to 70° C. for an additional 15 h
  3. temperatureThe reaction was cooled to room temperature
  4. customexcess base was consumed by the addition of a saturated aqueous solution of NH4Cl
  5. additionThe mixture was diluted with H2O
  6. washwashed with CH2Cl2
  7. dry with materialThe combined organic phase was dried over anhydrous Na2SO4
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by flash silica gel chromatography