Reaction equation
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]Participants
3
Conditions
- Temperature
- 70 °C
Procedure
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 %.
Workup
- customIn a four necked 100 ml flask equipped with a condenser, a dropping funnel
- customwas continued at the same temperature as above for 2 hours
- stirringwhile stirring
- washwas washed with an alkaline solution
- customdried with alumina
- temperaturecooled
Sources & evidence
- ORD record
- ord-6feb3db340634c9abaad56854f866c27
- Source dataset
- uspto-grants-1988_08
- Patent number
- US04766238
Linked notes
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