反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
产物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
At first, a mixture of the 4-(diallylethoxysilyl)iodobenzene (187 mg, 0.52 mmol) obtained in Example 2, Pd(PPh3)4 (18.1 mg, 0.016 mmol), K2CO3 (108 mg, 0.78 mmol), and 4-methoxyphenyl boronic acid (95.2 mg, 0.63 mmol) was added with dist.toluene (5 mL). Subsequently, the resultant mixture was stirred under a nitrogen atmosphere at 80° C. for 13 hours to obtain a reaction mixture. Thereafter, a salt formed in the reaction mixture was removed by filtering with celite. The solvent was distilled from the organic layer with an evaporator to obtain a crude product. After that, the crude product thus obtained was separated and purified by silica gel column chromatography (hexane/EtOAc=10/1), and thereby 4-(diallylethoxysilyl)-4′-methoxybiphenyl was obtained (157.3 mg, 89% yield).
WORKUP
后处理
- additionwas added with dist
- customto obtain a reaction mixture
- customThereafter, a salt formed in the reaction mixture
- customwas removed
- filtrationby filtering with celite
- distillationThe solvent was distilled from the organic layer with an evaporator
- customto obtain a crude product
- customAfter that, the crude product thus obtained
- customwas separated
- custompurified by silica gel column chromatography (hexane/EtOAc=10/1)