反应 #417948

ord-9d2bb70262ba419b9dad22782050253a

反应方程式

Oc1ccc(Br)nc1
2-bromo-5-hydroxypyridine
CCCBr
1-bromopropane
O=C([O-])[O-].[K+].[K+]
K2CO3
CCCOc1ccc(Br)nc1
2-Bromo-5-propoxy-pyridine

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度at reflux over night
  2. 2
    其他Afterwards the reaction is quenched by the addition of water
  3. 3
    萃取extracted with TBME
  4. 4
    干燥dried over MgSO4
  5. 5
    过滤filtered
  6. 6
    其他the solvent is removed in vacuo
  7. 7
    其他The crude product is purified by column chromatography (silica gel, PE/EtOAc)

实验过程

10.0 g (57.5 mmol) 2-bromo-5-hydroxypyridine, 28.3 g (230 mmol) 1-bromopropane and 19.9 g (143.7 mmol) K2CO3 are added to 1 L ACN and stirred at reflux over night. Afterwards the reaction is quenched by the addition of water and extracted with TBME. The org. layers are combined, dried over MgSO4, filtered and the solvent is removed in vacuo. The crude product is purified by column chromatography (silica gel, PE/EtOAc).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08877741B2uspto-grants-2014_11