反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
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
- stirringthe mixture was stirred overnight at 70° C
- temperatureThe reaction mixture was cooled to room temperature
- customwas quenched by the addition of 5 mL of water
- additionAqueous 1N HCl (5 mL) was added
- additionthe mixture was diluted with dichloromethane
- washThe organic layer was washed with saturated brine
- dry with materialdried over Na2SO4
- customdried in vacuo
- customThe crude product was purified on a Biotage (Biotage Inc.) 50 g silica column
- washeluting with 0-40% EtOAc in heptane over 40 minutes