Reacción #2267

ord-a6ba3063855543d494bab226d66b41f6

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

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

Procedimiento

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 at atmospheric pressure from 64°-68° C. to yield 36 g (79%) of a colorless liquid as pure product.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05728715uspto-grants-1998_03