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 an argon-purged and evacuated slurry of 910 mg (3.21 mmol) of 5-bromo-2-iodopyridine and 436 mg (3.21 mmol, 1.0 eq.) of 2-o-tolylboronic acid in 8 mL of toluene and 3.2 mL of 2 M aqueous sodium carbonate, was added 36 mg (0.032 mmol, 0.01 eq) of tetrakis(tri-phenylphosphine)palladium. The reaction mixture was purged and evacuated with argon twice more and then set to reflux under argon for 15 h. The reaction was cooled and partitioned between water and EtOAc. The layers were separated, and the aqueous layer extracted once more with EtOAc. The organic extracts were combined, dried over magnesium sulfate, filtered, concentrated and dried in vacuo to give the crude product as an orange oil. Purification by silica gel chromatography (7:3 CH2Cl2/hexanes) provided the title compound as a yellow oil, 666 mg, 84% yield.
WORKUP
后处理
- customTo an argon-purged
- customThe reaction mixture was purged
- customevacuated with argon twice more
- temperatureto reflux under argon for 15 h
- temperatureThe reaction was cooled
- custompartitioned between water and EtOAc
- customThe layers were separated
- extractionthe aqueous layer extracted once more with EtOAc
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customdried in vacuo
- customto give the crude product as an orange oil
- customPurification by silica gel chromatography (7:3 CH2Cl2/hexanes)