HRID1369965

反应详情

EQUATION

反应方程式

HRID 1369965 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
80 °C

PROCEDURE

实验过程

5.00 g of methyl 4-fluorobenzoylacetate (24.2 mmol, concentration 95%) and 1.69 g of isobutyronitrile (24.2 mmol, concentration 98%) were dissolved in 25 ml of toluene and treated with 7.01 g of tin tetrachloride (26.6 mmol, concentration >99%) at room temperature after the course of 10 minutes. After 3 h at room temperature, the mixture was heated to 80° C. After 11.5 h, the suspension was again cooled to room temperature and treated with 25 ml of water. The mixture was diluted with 10 ml of ethyl acetate and the phases were separated. The organic phase was washed twice with 10 ml of 1N sodium hydroxide solution and concentrated in vacuo (40° C./25 mbar) after drying over magnesium sulphate. 6.18 g of crude product were obtained in the form of a yellow oil. After chromatography on silica gel (eluent: hexane/ethyl acetate 1.5:1), 3.84 g of methyl 3-amino-2-[1-(4-fluorophenyl)methanoyl]-4-methylpent-2-enoate were obtained in the form of an oil.

WORKUP

后处理

  1. waitAfter 11.5 h
  2. temperaturethe suspension was again cooled to room temperature
  3. customthe phases were separated
  4. washThe organic phase was washed twice with 10 ml of 1N sodium hydroxide solution
  5. concentrationconcentrated in vacuo (40° C./25 mbar)
  6. dry with materialafter drying over magnesium sulphate
  7. custom6.18 g of crude product were obtained in the form of a yellow oil