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
- 7.5 °C
PROCEDURE
实验过程
Under nitrogen, 16.26 g (0.06 mol) of 3-[6-(2-fluoro-phenyl) -pyridin-3-yl]-acrylic acid ethyl ester were dissolved in 500 ml of 95% ethanol and cooled to 5 to 10° C. After addition of 9.42 g (0.03 mol) of bismuth trichloride, a total of 9.12 g (0.24 mol) of sodium borohydride was added in portions over 45 min. The resulting mixture was stirred at 15 to 20° C. for 1 h, then cooled to 10° C. and poured onto ice/water. The pH was adjusted to 7 with 2 N hydrochloric acid, dichloromethane was added, and the precipitated salts were separated by filtration. The organic phase of the mother liquor was separated, and the aqueous phase extracted once with dichloromethane. The combined organic phases were washed with a saturated sodium chloride solution, dried over sodium sulfate, filtered and evaporated to dryness. The remaining solid was purified by chromatography (silica gel, n-heptane/ethyl acetate 3:1). Yield: 11.5 g.
WORKUP
后处理
- temperaturecooled to 10° C.
- additionpoured onto ice/water
- additionwas added
- customthe precipitated salts were separated by filtration
- customThe organic phase of the mother liquor was separated
- extractionthe aqueous phase extracted once with dichloromethane
- washThe combined organic phases were washed with a saturated sodium chloride solution
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customevaporated to dryness
- customThe remaining solid was purified by chromatography (silica gel, n-heptane/ethyl acetate 3:1)