تفاعل #93258

ord-7bf644b4bd88429081a5dd32012016c8

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwhile cooling with ice
  2. 2
    أخرىdoes not exceed 15° C
  3. 3
    workup.STIRRINGThe mixture is stirred at about 15° C. for 2 hours
  4. 4
    أخرىthe organic phase is separated off
  5. 5
    استخلاصthe aqueous phase is subsequently extracted with methylene chloride
  6. 6
    غسيلThe methylene chloride solution is washed with water
  7. 7
    تجفيفdried with sodium sulphate
  8. 8
    workup.DISTILLATIONthe diluent is distilled off in vacuo
  9. 9
    درجة الحرارةThe residue (44 g) is heated at 130°-140° C. with 0.1 g of triphenylphosphine until the initially vigorous evolution of gas
  10. 10
    أخرى(about 45 minutes)
  11. 11
    workup.DISTILLATIONDistillation in vacuo

الإجراء التجريبي

25 g of 2,4,5-trifluorobenzoyl chloride in 10 ml of methylene chloride and 37.5 g of 1,1-dichloroethylene are successively added dropwise to a suspension of 18.5 g of anhydrous aluminum chloride in 75 ml of dry methylene chloride, while cooling with ice and stirring, during which the temperature does not exceed 15° C. The mixture is stirred at about 15° C. for 2 hours, is allowed to come to room temperature overnight and is poured onto a mixture of 150 g of ice and 15 ml of concentrated hydrochloric acid, the organic phase is separated off and the aqueous phase is subsequently extracted with methylene chloride. The methylene chloride solution is washed with water and dried with sodium sulphate and the diluent is distilled off in vacuo. The residue (44 g) is heated at 130°-140° C. with 0.1 g of triphenylphosphine until the initially vigorous evolution of gas has ended (about 45 minutes). Distillation in vacuo gives 23.8 g (72.8%) of 2,2-dichlorovinyl 2,4,5-trifluorophenyl ketone of boiling point 132° -134° C./14 mbar.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04611080uspto-grants-1986_09