Sodium Iodide → 4-[(Trifluoroethenyl)oxy]phenol
Reaction equation
[F:1][C:2]([O:6][C:7]1[CH:12]=[CH:11][C:10]([O:13]C)=[CH:9][CH:8]=1)=[C:3]([F:5])[F:4].C[Si](C)(C)Cl.[I-].[Na+]>C(#N)C>[F:1][C:2]([O:6][C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1)=[C:3]([F:5])[F:4]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A sample of 4-trifluoroethenyloxyanisole prepared as in Example 2 is treated with two equivalents of trimethylchlorosilane and sodium iodide in refluxing acetonitrile to give 4-trifluoroethenyloxyphenol. The product is extracted with ether, washed with sodium thiosulfate solution to remove iodine, and then concentrated by rotary evaporation.
Sources & evidence
- ORD record
- ord-c3e943254b1c4024ac255d81f55c27e0
- Source dataset
- uspto-grants-1991_08
- Patent number
- US05037919
Reaction notes
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