StartseiteMCPWorkbenchSkills
StartseiteWorkbenchBenachrichtigungenMein Bereich
llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
  1. Startseite
  2. /Reaktion

Vinylidene chloride → 1,1,1-Trifluoro-4,4-dichloro-3-buten-2-one

HRID 238675
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 238675
[Cl-].[Al+3].[Cl-].[Cl-].[F:5][C:6]([F:11])([F:10])[C:7](Cl)=[O:8].[C:12]([Cl:15])([Cl:14])=[CH2:13]>ClCCl.O>[Cl:14][C:12]([Cl:15])=[CH:13][C:7](=[O:8])[C:6]([F:11])([F:10])[F:5]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 6366Vinylidene chlorideHCID 61106Trifluoroacetyl chlorideHCID 6451240Aluminum(III) Chloride

Produkt 1

HCID 155483241,1,1-Trifluoro-4,4-dichloro-3-buten-2-one

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6344Dichloromethane
Lösungsmittel
3×

Reaktionsbedingungen

Temperatur
-50 °C

Versuchsvorschrift

To a solution of aluminum chloride (3.0 g, 22.5 mmol) in dichloromethane (100 mL) was added dropwise a solution of trifluoroacetyl chloride (3 g, 22.6 mmol) in dichloro-methane (5 mL) while keeping the temperature of the reaction mixture below −30° C. The reaction mixture was stirred for 15 minutes at −50° C. Then a solution of vinylidene chloride (2.2 g, 22.7 mmol) in dichloromethane (10 mL) was added dropwise over 2 h to the reaction mixture. The reaction mixture was stirred an additional 2 h at −50° C. and then warmed gradually to room temperature. The reaction mixture was diluted with water, and the aqueous layer was extracted with dichloromethane. The organic layers were combined, dried (MgSO4), and concentrated under reduced pressure to give 4,4-dichloro-1,1,1-trifluoro-3-buten-2-one as an oil which was used for the next step without further purification.

Aufarbeitung

  1. customthe temperature of the reaction mixture below −30° C
  2. stirringThe reaction mixture was stirred an additional 2 h at −50° C.
  3. temperaturewarmed gradually to room temperature
  4. extractionthe aqueous layer was extracted with dichloromethane
  5. dry with materialdried (MgSO4)
  6. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-47e546a997ae40af86e9cfaeef5e35a7
Quelldatensatz
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08642634B2

Notizen zur Reaktion

Wird geladen…

Auf dieser SeiteKomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion