Reaktion #42131

ord-41cf697fc97a4e12acff528e5f786692

Reaktionsgleichung

CCO
ethanol
O=S(=O)(O)Cl
chlorosulfuric acid
FC(F)=CC(F)(F)F
1,1,3,3,3-pentafluoropropene
CCOC(=O)CC(F)(F)F
CF3CH2COOEt
Ausbeute 87.0%

Reaktionsbedingungen

Temperatur
20°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturcooled in liquid nitrogen
  2. 2
    Sonstigeevacuated
  3. 3
    Temperaturto warm
  4. 4
    workup.ADDITIONthe reaction mixture was added drop by drop into the flask
  5. 5
    SonstigeThe organic layer was separated
  6. 6
    Waschenwashed with sodium bicarbonate, water
  7. 7
    Sonstigedried under MgSO4
  8. 8
    workup.DISTILLATIONDistillation

Vorschrift

A 100 mL Hastelloy shaker tube was loaded with 26.5 g (0.227 mole) chlorosulfuric acid, cooled in liquid nitrogen, evacuated and loaded with 30 g (0.225 mole) of 1,1,3,3,3-pentafluoropropene. The reaction vessel was allowed to warm and kept on a shaker at 40° C. at autogenous pressure for 6 hours. The pressure tube was unloaded, and the reaction mixture was added drop by drop into the flask containing 60 ml of ethanol at −10° C. over a 15 minute period. The reaction mixture was stirred overnight at 20° C. and then was poured into 200 ml of ice water. The organic layer was separated, washed with sodium bicarbonate, water, and dried under MgSO4. Distillation gave 31 g of CF3CH2COOEt (87%), bp 108-109° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728183B2uspto-grants-2010_06