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
CONDITIONS
反应条件
- 温度
- 110 °C
PROCEDURE
实验过程
To a solution of 150 g of 2-chloro-5-fluoropyridin-3-amine in 600 mL of N,N-dimethylformamide, 190 mL of butyl acrylate and 287 mL of triethylamine were added under a nitrogen flow, and the mixture was stirred at 110° C. for 2 hours. The reaction mixture was cooled to 58° C., thereto were added 13.1 g of bis(tri-tert-butylphosphine)palladium(0), and the mixture was stirred at 110 to 120° C. for 40 minutes. The reaction mixture was cooled to 57° C., 13.1 g of bis(tri-tert-butylphosphine)palladium(0) was added thereto, and the mixture was stirred at 110 to 120° C. for 3 hours. The reaction mixture was cooled to room temperature, and water and ethyl acetate were added thereto. The insoluble substance was filtered off, the organic layer of the filtrate was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and the extract were combined, the resultant solution was washed sequentially with water and a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Cyclohexane and ethyl acetate were added to the resultant residue, and the solid was filtered off to obtain 200 g of butyl (2E)-3-(3-amino-5-fluoropyridin-2-yl)acrylate as a light brown solid.
WORKUP
后处理
- temperatureThe reaction mixture was cooled to 58° C.
- stirringthe mixture was stirred at 110 to 120° C. for 40 minutes
- temperatureThe reaction mixture was cooled to 57° C.
- stirringthe mixture was stirred at 110 to 120° C. for 3 hours
- temperatureThe reaction mixture was cooled to room temperature
- filtrationThe insoluble substance was filtered off
- customthe organic layer of the filtrate was separated
- extractionthe aqueous layer was extracted with ethyl acetate
- washthe resultant solution was washed sequentially with water
- dry with materiala saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate
- distillationthe solvent was distilled off under reduced pressure
- additionCyclohexane and ethyl acetate were added to the resultant residue
- filtrationthe solid was filtered off