反应 #1135809

ord-ebe6b4479277463cbb3ea1e6aa207453

反应方程式

O=C(CBr)c1c(F)c(F)c(F)c(F)c1F
1-(2,3,4,5,6-pentafluorophenyl)-2-bromo-1-ethanone
N#C[S-].[NH4+]
ammonium thiocyanate
O=C([O-])O.[Na+]
sodium bicarbonate
N#CSCC(=O)c1c(F)c(F)c(F)c(F)c1F
1-(2,3,4,5,6-pentafluorophenyl)-2-thiocyanato-1-ethanone

反应条件

温度
25°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他To the reaction mixtures
  2. 2
    萃取the mixtures were extracted with ethyl acetate
  3. 3
    洗涤The organic layers were washed with aqueous saturated sodium bicarbonate solution
  4. 4
    干燥were dried over anhydrous sodium sulfate
  5. 5
    浓缩The resulting mixtures were concentrated under reduced pressure

实验过程

A mixture of 1-(2,3,4,5,6-pentafluorophenyl)-2-bromo-1-ethanone 5.00 g, ammonium thiocyanate 1.58 g and acetonitrile 100 mL was stirred at 25° C. for one hour. To the reaction mixtures was added aqueous saturated sodium bicarbonate solution and the mixtures were extracted with ethyl acetate. The organic layers were washed with aqueous saturated sodium bicarbonate solution and were dried over anhydrous sodium sulfate. The resulting mixtures were concentrated under reduced pressure to give 1-(2,3,4,5,6-pentafluorophenyl)-2-thiocyanato-1-ethanone.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09380782B2uspto-grants-2016_07