反应 #684972

ord-866169d0aa594cd2ad7e6027e71e9945

反应方程式

CCOC(C)=O
ethyl acetate
O=C([O-])[O-].[K+].[K+]
Potassium carbonate
CI
methyl iodide
CCCCc1ccc(Cc2ncccc2O)cc1
compound
CCCCc1ccc(Cc2ncccc2O)cc1
2-(4-Butylbenzyl)-3-pyridinol
CCCCc1ccc(Cc2ncccc2OC)cc1
title compound
收率 7.2%
CCCCc1ccc(Cc2ncccc2OC)cc1
2-(4-Butylbenzyl)-3-methoxypyridine
收率 7.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤the reaction mixture was washed with saturated brine
  2. 2
    浓缩concentrated under reduced pressure
  3. 3
    其他The residue was purified by silica gel column chromatography

实验过程

Potassium carbonate (33.0 mg, 0.239 mmol) and methyl iodide (14.9 μl, 0.239 mmol) were added to a solution of the compound of Example B230 (19.2 mg, 0.0796 mmol) in acetone (1 ml), and this reaction mixture was stirred at room temperature for 3 hours. After ethyl acetate was added, the reaction mixture was washed with saturated brine and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (1.47 mg).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07897387B2uspto-grants-2011_03