(3-Chloro-5-(trifluoromethyl)phenyl)methanol → [3-Bromo-5-(trifluoromethyl)phenyl]methanol
Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([C:12]([F:15])([F:14])[F:13])[CH:11]=1)[C:5](OC)=[O:6].ClC1C=C(CO)C=C(C(F)(F)F)C=1>>[Br:1][C:2]1[CH:3]=[C:4]([CH2:5][OH:6])[CH:9]=[C:10]([C:12]([F:14])([F:15])[F:13])[CH:11]=1Participants
3
Procedure
The title compound was prepared from methyl 3-bromo-5-(trifluoromethyl)benzoate (Reference Example 37) by a procedure similar to the one described for (3-chloro-5-(trifluoromethyl)phenyl)methanol (Reference Example 30) to provide (3-bromo-5-(trifluoromethyl)phenyl)methanol (7.42 g, 35% (2 steps)) as a yellow oil.
Sources & evidence
- ORD record
- ord-e6c46743bfe84d0ca0ba5b422a1fe056
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08853215B2
Reaction notes
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