Reaktion #2167

ord-08d5189834b7446baa12a49af6278da7

Reaktionsgleichung

FC1(F)CC(Cl)(Cl)C1(F)Cl
1,1,2 trichloro-2,3,3-trifluorocyclobutane
O
H2O
Cl
HCl
FC1(F)C=C(Cl)C1(F)Cl
colorless liquid
Ausbeute 79.0%
FC1(F)C=C(Cl)C1(F)Cl
1,4-dichloro-1,2,2-trifluorocyclobut-3-ene
Ausbeute 79.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    WaschenThe ether layer was washed with H2O (100 ml), brine (100 ml)
  2. 2
    Trocknendried over anhydrous MgSO4
  3. 3
    Sonstigeevaporated in vacuo
  4. 4
    workup.DISTILLATIONThe residue was distilled fractionally atmospheric pressure from 64°-68° C.

Vorschrift

To a solution of 1,1,2 trichloro-2,3,3-trifluorocyclobutane (55.5 g) in 100 ml of anhydrous ether, triethylamine (40 ml) was added dropwise over 30 min at room temperature, and the mixture was stirred overnight at ambient temperature. The mixture was then stirred with 120 ml H2O and 7.5 ml of concentrated HCl. The ether layer was washed with H2O (100 ml), brine (100 ml), dried over anhydrous MgSO4, and evaporated in vacuo. The residue was distilled fractionally atmospheric pressure from 64°-68° C. to yield 36 g (79%) of a colorless liquid as pure product.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728694uspto-grants-1998_03