Hydrochloric Acid → 2,2-Dichlorovinyl 2,4,5-trifluorophenyl ketone

HRID 64980

Reaktionsgleichung

Reaktionsgleichung von HRID 64980
[F:1][C:2]1[CH:10]=[C:9]([F:11])[C:8]([F:12])=[CH:7][C:3]=1[C:4](Cl)=[O:5].[Cl:13][C:14]([Cl:16])=[CH2:15].[Cl-].[Al+3].[Cl-].[Cl-].Cl>C(Cl)Cl>[F:1][C:2]1[CH:10]=[C:9]([F:11])[C:8]([F:12])=[CH:7][C:3]=1[C:4]([CH:15]=[C:14]([Cl:16])[Cl:13])=[O:5]

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 6366Vinylidene chlorideHCID 1451642,4,5-Trifluorobenzoyl chlorideHCID 6451240Aluminum(III) Chloride

Produkt 1

HCID 202362462,2-Dichlorovinyl 2,4,5-trifluorophenyl ketoneAusbeute 72,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

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.

Aufarbeitung

  1. temperaturewhile cooling with ice
  2. customdoes not exceed 15° C
  3. stirringThe mixture is stirred at about 15° C. for 2 hours
  4. customthe organic phase is separated off
  5. extractionthe aqueous phase is subsequently extracted with methylene chloride
  6. washThe methylene chloride solution is washed with water
  7. dry with materialdried with sodium sulphate
  8. distillationthe diluent is distilled off in vacuo
  9. temperatureThe residue (44 g) is heated at 130°-140° C. with 0.1 g of triphenylphosphine until the initially vigorous evolution of gas
  10. custom(about 45 minutes)
  11. distillationDistillation in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-7bf644b4bd88429081a5dd32012016c8
Quelldatensatz
uspto-grants-1986_09
Patentnummer
US04611080

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