反应 #1876812

ord-e2b1c3cd2a7f482abbd02b5942d73d0c

反应方程式

BrBr
Bromine
CCOc1cccc(C(F)(F)F)c1
Compound ( b )
CCOc1cccc(C(F)(F)F)c1
3-ethoxybenzotrifluoride
O
Water
CCOc1ccc(Br)c(C(F)(F)F)c1
Compound ( c )
收率 76.9%
CCOc1ccc(Br)c(C(F)(F)F)c1
2-bromo-5-ethoxybenzotrifluoride
收率 76.9%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取the aqueous layer was extracted three times with ether
  2. 2
    洗涤washed with saturated aqueous sodium bicarbonate and water
  3. 3
    干燥dried over anhydrous magnesium sulfate
  4. 4
    workup.DISTILLATIONThe solvent was distilled off under reduced pressure

实验过程

Bromine (18.2 g) was slowly added dropwise to Compound (b) (19.3 g) at room temperature, and then the mixture was stirred at room temperature for 1 hour. Water and ether were added for liquid separation, and the aqueous layer was extracted three times with ether. The organic layers were combined, washed with saturated aqueous sodium bicarbonate and water, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain 21.0 g of Compound (c).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07070838B2uspto-grants-2006_07