反应 #1147

反应方程式

Sodium hydride

6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran-2-carbaldehyde

diethyl cyanomethylphosphonate

hydrochloric acid

→

2-(2-cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran

收率 83.1%

溶剂

N,N-dimethylformamide

反应条件

后处理

1. 1
   萃取followed by extraction with ethyl acetate (200 ml)
2. 2
   洗涤After the ethyl acetate layer was washed with water
3. 3
   干燥dried (MgSO4), palladium-carbon (5%, 0.70 g)
4. 4
   workup.ADDITIONwas added
5. 5
   其他followed by catalytic reduction at room temperature under an atmospheric pressure of 1 atm
6. 6
   过滤After the catalyst was filtered off
7. 7
   浓缩the filtrate was concentrated
8. 8
   洗涤From the fraction eluted with ethyl acetate-chloroform (2:98

实验过程

Sodium hydride (60%, oily, 0.20 g) was gradually added to a solution of 6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran-2-carbaldehyde (1.50 g) and diethyl cyanomethylphosphonate (0.88 g) in N,N-dimethylformamide (30 ml) at 0° C., followed by stirring at room temperature for 1 hour. The reaction mixture was poured over ice water and neutralized with 2N hydrochloric acid, followed by extraction with ethyl acetate (200 ml). After the ethyl acetate layer was washed with water and dried (MgSO4), palladium-carbon (5%, 0.70 g) was added, followed by catalytic reduction at room temperature under an atmospheric pressure of 1 atm. After the catalyst was filtered off, the filtrate was concentrated; the residue was subjected to silica gel column chromatography. From the fraction eluted with ethyl acetate-chloroform (2:98, v/v), crystals of 2-(2-cyanoethyl)-6-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzofuran (1.34 g, 83%) were obtained, which was then recrystallized from dichloromethane-hexane to yield colorless prisms having a melting point of 92° to 93° C.

来源