Potassium Hydroxide → HCID 53986718, compound
Reaction equation
[C:1]1([CH:7](Cl)[CH:8]([C:10]([F:13])([F:12])[F:11])[CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[K+]>C(O)C>[C:1]1([CH:7]=[C:8]([C:10]([F:11])([F:12])[F:13])[CH3:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To 7 ml of ethanol added was 0.6 mmol (0.126 g) of 1-phenyl-1-chloro-2-trifluoromethylpropane, and then 2 mmol (0.112 g) of potassium hydroxide was added thereto and allowed to react at 50° C. for 18 hours, whereby 1-phenyl-2-trifluoromethylpropene was obtained at a yield of 71%. The results of analyses of the product are shown below.
Workup
- customto react at 50° C. for 18 hours
Sources & evidence
- ORD record
- ord-664e6ee2a23e447ca131408120f80e9d
- Source dataset
- uspto-grants-1992_06
- Patent number
- US05118879
Reaction notes
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