反应 #1192

ord-31b708e4b55e4146a82a5bb5a9af3de8

反应方程式

CCCCC(CC)CBr
2-ethylhexyl bromide
OCCCCCCCCCCO
1,10-decanediol
[K+].[OH-]
KOH
CCCCC(CC)COCCCCCCCCCCO
10-(2-ethylhexyloxy)decanol
收率 72.1%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他A 1-liter flask equipped with a stirrer
  2. 2
    workup.DISTILLATIONdistilling off water
  3. 3
    其他formed
  4. 4
    温度the resulting mixture was heated
  5. 5
    其他After completion of the reaction
  6. 6
    洗涤washed with water
  7. 7
    workup.DISTILLATIONAfter the solvent was distilled off under reduced pressure
  8. 8
    其他the resulting residue was purified by column chromatography on silica gel

实验过程

A 1-liter flask equipped with a stirrer and distiller was charged with 25 g (0.14 mol) of 1,10-decanediol, 8.09 g (0.14 mol) of KOH and 300 ml of xylene, and the resultant mixture was heated at 120° C. for 1 hour, thereby distilling off water formed. To this reaction mixture, were added 23.1 g (0.12 mol) of 2-ethylhexyl bromide, and the resulting mixture was heated and stirred for 15 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and washed with water. After the solvent was distilled off under reduced pressure, the resulting residue was purified by column chromatography on silica gel, thereby obtaining 24.8 g (yield: 72%) of 10-(2-ethylhexyloxy)decanol.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723497uspto-grants-1998_03