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 2-bromo-5-(methoxymethoxy)pyridine (30.5 g, 140 mmol) in THF (5 mL) at 0° C. under N2 is added dichloro-((bis-diphenylphosphino)ferrocenyl)-palladium(II) (4.88 g, 5.5 mmol) followed by dropwise addition of neopentylmagnesium chloride (155 mL, 155 mmol) over 2 min. After addition, the cooling bath was removed and the reaction stirred 3 h at rt. The reaction was cooled to 0° C. and saturated NH4Cl (500 mL) was added, and the aqueous layers extracted with EtOAc (3×200 mL). The combined organic layers were washed with saturated NaCl, dried (Na2SO4) and concentrated to give a red oil. Purification by vacuum filtration through a silica plug (9×7 cm, dry load, 10-20%% EtOAc/Hexanes) gives 5-(methoxymethoxy)-2-neopentylpyridine as a light yellow oil.
WORKUP
后处理
- additionAfter addition
- customthe cooling bath was removed
- temperatureThe reaction was cooled to 0° C.
- additionsaturated NH4Cl (500 mL) was added
- extractionthe aqueous layers extracted with EtOAc (3×200 mL)
- washThe combined organic layers were washed with saturated NaCl
- dry with materialdried (Na2SO4)
- concentrationconcentrated
- customto give a red oil
- customPurification
- filtrationby vacuum filtration through a silica plug (9×7 cm, dry load, 10-20%% EtOAc/Hexanes)