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
- 70 °C
PROCEDURE
实验过程
3-Methyl-6-bromo-oxazolo[4,5-b]pyridin-2(3H)-one (2.58 g) (0.012 mole) in 80 ml of benzene is treated with 365 mg tri-o-tolylphosphine, 138 mg palladium acetate, 1.87 g (0.018 mole) of isopropenyl acetate and 5.9 g (0.18 mole) of tributyltin methoxide. This is sealed in a high pressure tube and heated to 70° C. for 25 hours. The reaction mixture is then quenched with 20 ml sat. ammonium chloride and diluted with 50 ml ethyl acetate. The organic phase separates, dried over sodium sulfate and concentrated to dryness. The residue is dissolved in methylene chloride, washed with sat. KF solution, filtered through a cotton plug, dried over sodium sulfate and concentrated to dryness to obtain crude product. This is chromatographed using 200×60 mm SiO2, EtOAc (100%) as eluent. The desired product is identified by NMR and used directly in the next step.
WORKUP
后处理
- customThis is sealed in a high pressure tube
- customThe reaction mixture is then quenched with 20 ml sat. ammonium chloride
- additiondiluted with 50 ml ethyl acetate
- dry with materialThe organic phase separates, dried over sodium sulfate
- concentrationconcentrated to dryness
- dissolutionThe residue is dissolved in methylene chloride
- washwashed with sat. KF solution
- filtrationfiltered through a cotton plug
- dry with materialdried over sodium sulfate
- concentrationconcentrated to dryness
- customto obtain crude product
- customThis is chromatographed