반응 #65853

ord-d51b4843b81c4750bed4bae0a1c962bc

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe reaction mixture was subsequently stirred at room temperature until the evolution of gas
  2. 2
    기타the phases were separated
  3. 3
    추출the aqueous phase was extracted with chloroform
  4. 4
    세척The combined organic phases were washed with ice-water and sodium hydrogencarbonate solution
  5. 5
    건조dried over magnesium sulphate
  6. 6
    기타the readily volatile components were removed on a rotary evaporator

실험 절차

136 g of 2-(2,2,2-trifluoroethyl)-2-trifluoromethyl-1,3-benzodioxole were dissolved in 125 ml of chloroform. 175 g of chlorosulphonic acid were added dropwise at 0° C., with stirring, and the reaction mixture was subsequently stirred at room temperature until the evolution of gas had ended. It was then poured into 750 g of ice-water, the phases were separated and the aqueous phase was extracted with chloroform. The combined organic phases were washed with ice-water and sodium hydrogencarbonate solution and dried over magnesium sulphate and the readily volatile components were removed on a rotary evaporator to give 133 g of product (=72% of theory). The melting point was 55° to 57° C. 19F NMR: -60.8 and -86.5 ppm. 1H NMR: 3.13 ppm.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05420309uspto-grants-1995_05