Trimethyl borate → 2-Fluoro-3-(pyridin-3-yl)phenylboronic acid
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=1.[B:14](OC)([O:17]C)[O:15]C>>[F:1][C:2]1[C:3]([C:8]2[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=2)=[CH:4][CH:5]=[CH:6][C:7]=1[B:14]([OH:17])[OH:15]Participants
3
Procedure
3-(2-Fluorophenyl)pyridine was lithiated and reacted with trimethyl borate as described in Example 31 to give 2-fluoro-3-(pyridin-3-yl)benzeneboronic acid as a white solid: m/z (ES+) 218 (M++H).
Sources & evidence
- ORD record
- ord-1e80b2503fee485a99dbf375bc844f90
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06900215B2
Reaction notes
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