Reaktion #1135809

ord-ebe6b4479277463cbb3ea1e6aa207453

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Temperatur
25°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeTo the reaction mixtures
  2. 2
    Extraktionthe mixtures were extracted with ethyl acetate
  3. 3
    WaschenThe organic layers were washed with aqueous saturated sodium bicarbonate solution
  4. 4
    Trocknenwere dried over anhydrous sodium sulfate
  5. 5
    EinengenThe resulting mixtures were concentrated under reduced pressure

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09380782B2uspto-grants-2016_07