Methanol → (4-Iodo-2-(trifluoromethyl)phenyl)methanol
Reaction equation
[I:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](O)=[O:7])=[C:4]([C:11]([F:14])([F:13])[F:12])[CH:3]=1.CO>C1COCC1>[I:1][C:2]1[CH:10]=[CH:9][C:5]([CH2:6][OH:7])=[C:4]([C:11]([F:12])([F:13])[F:14])[CH:3]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
To a solution of 4-iodo-2-(trifluoromethyl)benzoic acid (for a preparation see Intermediate 31)(16.7 g, 52.8 mmol) in THF (150 ml) at ambient temperature under nitrogen was added 1.0 M borane-tetrahydrofuran complex (100 ml, 100 mmol, Aldrich) dropwise. The solution was heated to 80° C. for 1.5 h. To the solution at ambient temperature was added methanol (75 ml) and then heated to 80° C. for 1 h. The solvent was removed in vacuo to leave a mobile oil. The residue was partitioned between ethyl acetate (200 ml) and 2 N aqueous HCl (100 ml). The phases were separated and the organic phase washed with 2 N aqueous sodium hydroxide (100 ml), brine (50 ml), then dried (MgSO4), filtered and the solvent removed in vacuo to give [4-iodo-2-(trifluoromethyl)phenyl]methanol as a pale brown solid (14.8 g).
Workup
- customat ambient temperature
- additionwas added 1.0 M borane-tetrahydrofuran complex (100 ml, 100 mmol, Aldrich) dropwise
- temperatureheated to 80° C. for 1 h
- customThe solvent was removed in vacuo
- customto leave a mobile oil
- customThe residue was partitioned between ethyl acetate (200 ml) and 2 N aqueous HCl (100 ml)
- customThe phases were separated
- washthe organic phase washed with 2 N aqueous sodium hydroxide (100 ml), brine (50 ml)
- dry with materialdried (MgSO4)
- filtrationfiltered
- customthe solvent removed in vacuo
Sources & evidence
- ORD record
- ord-5b67c105aae14239811ad355b86de5e8
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399436B2
Reaction notes
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