HRID2359302
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
4-bromo-2-chlorophenol (1.0 g, 4.8 mmol) was dissolved in DMF (35 ml) and water (5 ml) was added followed by sodium chloro(difluoro)acetate (2.0 g, 12 mmol) and cesium carbonate (3.1 g, 9.6 mmol). The mixture was stirred for 15 minutes at room temperature and then heated to 100° C. for 2 hours under nitrogen. The mixture was partitioned between water (50 ml) and tBuOMe (50 ml). The organic phase was separated, washed brine, dried over sodium sulphate, filtered, and concentrated in vacuo to give a crude product. The crude product was purified by silica gel chromatography eluting with 0-30% EtOAc in heptanes to give a title compound (0.83 g, 67% yield) as colourless oil.
WORKUP
后处理
- temperatureheated to 100° C. for 2 hours under nitrogen
- customThe mixture was partitioned between water (50 ml) and tBuOMe (50 ml)
- customThe organic phase was separated
- washwashed brine
- dry with materialdried over sodium sulphate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customto give a crude product
- customThe crude product was purified by silica gel chromatography
- washeluting with 0-30% EtOAc in heptanes