反应 #684969

ord-eed983d020be4ed8bef379b414531a3b

反应方程式

O
Water
CCOC(C)=O
ethyl acetate
Oc1nccc2ccccc12
1-hydroxyisoquinoline
BrBr
Bromine
Oc1ncc(Br)c2ccccc12
title compound
收率 80.1%
Oc1ncc(Br)c2ccccc12
4-Bromo-1-isoquinolinol
收率 80.1%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他the resulting reaction mixture
  2. 2
    过滤was filtered
  3. 3
    过滤through filter paper
  4. 4
    洗涤The organic layer was washed with saturated brine
  5. 5
    浓缩concentrated under reduced pressure
  6. 6
    其他The residue was recrystallized from ethyl acetate and hexane

实验过程

Bromine (1.78 ml, 34.5 mmol) was added to an ice-cooled solution of 1-hydroxyisoquinoline (5.01 g, 34.5 mmol) in acetic acid (50 ml), and this reaction mixture was stirred at room temperature for 2 hours. Water, ethyl acetate, and tetrahydrofuran were added, and the resulting reaction mixture was filtered through filter paper. The organic layer was washed with saturated brine and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate and hexane to give the title compound (6.19 g).

来源

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