Pyridine → 3,3,3-Trifluoro-2-(trifluoromethyl)-1-propene

HRID 35388

Reaktionsgleichung

Reaktionsgleichung von HRID 35388
N1C=CC=CC=1.[F:7][C:8]([F:20])([F:19])[CH:9]([C:15]([F:18])([F:17])[F:16])[C:10](OCCl)=O>>[F:7][C:8]([F:20])([F:19])[C:9]([C:15]([F:18])([F:17])[F:16])=[CH2:10]

Komponenten

3

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

In a four necked 100 ml flask equipped with a condenser, a dropping funnel and a thermometer, pyridine (19.3 g, 244 mmol) was charged and warmed to 70° C. Monochloromethyl 2-trifluoromethyl-3,3,3-trifluoropropanoate (4.88 g, 20 mmol) was dropwise added thereto while stirring. The reaction was continued at the same temperature as above for 2 hours while stirring. The gas evolved from a top of the condenser was washed with an alkaline solution, dried with alumina and cooled. The resultant liquid was distillated to give 2-trifluoromethyl-3,3,3-trifluoropropene (b.p., 14° C.) (2.30 g). Yield, 70 %.

Aufarbeitung

  1. customIn a four necked 100 ml flask equipped with a condenser, a dropping funnel
  2. customwas continued at the same temperature as above for 2 hours
  3. stirringwhile stirring
  4. washwas washed with an alkaline solution
  5. customdried with alumina
  6. temperaturecooled

Quellen und Nachweise

ORD-Eintrag
ord-6feb3db340634c9abaad56854f866c27
Quelldatensatz
uspto-grants-1988_08
Patentnummer
US04766238

Verknüpfte Notizen

Wird geladen…