反应 #66102

ord-203bea987b4746448a898a969cf61fa0

反应方程式

O=C(CBr)C1CCOCC1
2-bromo-1-(tetrahydro-pyran-4-yl)-ethanone
Cc1ccccn1
2-picoline
Cc1cccc[n+]1CC(=O)C1CCOCC1.[Br-]
2-methyl-1-[2-oxo-2-(tetrahydro-pyran-4-yl)-ethyl]-pyridinium bromide
收率 86.4%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度was heated
  2. 2
    温度to reflux
  3. 3
    温度maintained overnight
  4. 4
    其他The solvent was removed in vacuo
  5. 5
    其他to give a residue which
  6. 6
    洗涤was washed with 20% ethyl acetate in hexane

实验过程

A mixture of 2-bromo-1-(tetrahydro-pyran-4-yl)-ethanone (0.6 g, 2.89 mmol) and 2-picoline (0.4 mL, 4.3 mmol) in methanol (10 mL) was heated to reflux and maintained overnight. The solvent was removed in vacuo to give a residue which was washed with 20% ethyl acetate in hexane to afford 2-methyl-1-[2-oxo-2-(tetrahydro-pyran-4-yl)-ethyl]-pyridinium bromide (0.75 g, 86%) as a semi-solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08524705B2uspto-grants-2013_09