HRID1913426

反应详情

EQUATION

反应方程式

HRID 1913426 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Ethyl cyanoacetate (2.56 mL, 24.0 mmol) was added dropwise to a suspension of 959 mg of NaH (60%, 24.0 mmol) in 10 mL of DMF. The mixture was stirred for 1 h at room temperature. CsF (61 mg, 0.4 mmol) and a solution of 4-chloro-3-nitro-anisole (1.5 g, 8.0 mmol) in 2 mL of DMF were added and the mixture was stirred overnight at 70° C. The reaction mixture was cooled to room temperature and was quenched by the addition of 5 mL of water. Aqueous 1N HCl (5 mL) was added to adjust the pH to 3-4 and the mixture was diluted with dichloromethane. The organic layer was washed with saturated brine, dried over Na2SO4, and dried in vacuo. The crude product was purified on a Biotage (Biotage Inc.) 50 g silica column, eluting with 0-40% EtOAc in heptane over 40 minutes to provide 1.83 g (87%) of cyano-(4-methoxy-2-nitro-phenyl)-acetic acid ethyl ester.

WORKUP

后处理

  1. stirringthe mixture was stirred overnight at 70° C
  2. temperatureThe reaction mixture was cooled to room temperature
  3. customwas quenched by the addition of 5 mL of water
  4. additionAqueous 1N HCl (5 mL) was added
  5. additionthe mixture was diluted with dichloromethane
  6. washThe organic layer was washed with saturated brine
  7. dry with materialdried over Na2SO4
  8. customdried in vacuo
  9. customThe crude product was purified on a Biotage (Biotage Inc.) 50 g silica column
  10. washeluting with 0-40% EtOAc in heptane over 40 minutes