HRID453514

反应详情

EQUATION

反应方程式

HRID 453514 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

A flask was charged with tert-butyl 2-(3-cyano-4-fluorophenyl)acetate (9.410 g, 40.00 mmol), methyl 4-hydroxybenzoate (7.303 g, 48.00 mmol), K2CO3 (6.634 g, 48.00 mmol), and DMSO (160 mL). The mixture was heated to 90° C. under a nitrogen atmosphere for 17 hours. The mixture was cooled to ambient temperature and poured into a mixture of EtOAc (250 mL) and 10% K2CO3 solution (250 mL). The resulting insoluble residue was dissolved in water and added to the EtOAc-aqueous mixture. The mixture was stirred for 1 hour and layers were separated. The aqueous layer was extracted with EtOAc, and the combined extracts were washed with saturated K2CO3, water, and brine, dried over MgSO4, filtered through a Celite pad, and concentrated under reduced pressure to give 14.7 g of crude product as an oil. The crude material was purified by silica gel chromatography to provide methyl 4-(4-(2-tert-butoxy-2-oxoethyl)-2-cyanophenoxy)benzoate (11.6 g, 79%) as a white solid.

WORKUP

后处理

  1. temperatureThe mixture was cooled to ambient temperature
  2. customlayers were separated
  3. extractionThe aqueous layer was extracted with EtOAc
  4. washthe combined extracts were washed with saturated K2CO3, water, and brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered through a Celite pad
  7. concentrationconcentrated under reduced pressure
  8. customto give 14.7 g of crude product as an oil
  9. customThe crude material was purified by silica gel chromatography