反応 #1876812

ord-e2b1c3cd2a7f482abbd02b5942d73d0c

反応方程式

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 )
収率 76.9%
CCOc1ccc(Br)c(C(F)(F)F)c1
2-bromo-5-ethoxybenzotrifluoride
収率 76.9%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

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).

出典

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