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
To a solution of 3-iodo-4-nitroanisole (4.21 g, 15.1 mmol) in 1,2-dimethoxyethane (50 mL) were added 4,4,5,5-tetramethyl-2-(3,3,5,5-tetramethylcyclohex-1-enyl)[1,3,2]dioxaborolane (4.78 g, 18.1 mmol) produced in Example (4b), tripotassium phosphate (4.81 g, 22.7 mmol) and water (3 mL). Then, tetrakis(triphenylphosphine)palladium(0) (870 mg, 0.755 mmol) was added to the mixture while stirring at room temperature under a nitrogen atmosphere. The mixture was then further stirred for 13 hours at an external temperature of 70° C. To the reaction mixture were added tetrakis(triphenylphosphine)palladium(0) (870 mg, 0.755 mmol) and water (3 mL), followed by stirring for 26 hours at an external temperature of 100° C. The reaction mixture was cooled, and then ethyl acetate was added and the mixture was filtered through Celite. The filtrate was concentrated to give a residue, which was subjected to extraction with ethyl acetate, and the organic layer was washed with brine. The organic layer was dried over anhydrous magnesium sulfate and then the desiccant was filtered off and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (ethyl acetate/heptane) to give 1.5 g of the title compound as a yellow solid.
WORKUP
后处理
- stirringThe mixture was then further stirred for 13 hours at an external temperature of 70° C
- stirringby stirring for 26 hours at an external temperature of 100° C
- temperatureThe reaction mixture was cooled
- filtrationthe mixture was filtered through Celite
- concentrationThe filtrate was concentrated
- customto give a residue, which
- extractionwas subjected to extraction with ethyl acetate
- washthe organic layer was washed with brine
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate
- filtrationthe desiccant was filtered off
- concentrationthe filtrate was concentrated under reduced pressure
- customThe resultant residue was purified by silica gel column chromatography (ethyl acetate/heptane)