Sodium Hydroxide → 6-(4-Fluorophenyl)nicotinic acid
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:17]=[CH:16][C:11]([C:12]([O:14]C)=[O:13])=[CH:10][N:9]=2)=[CH:4][CH:3]=1.[OH-].[Na+]>>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:17]=[CH:16][C:11]([C:12]([OH:14])=[O:13])=[CH:10][N:9]=2)=[CH:4][CH:3]=1Participants
3
Procedure
In a similar manner to that described in Example 2, a reaction was carried out using methyl 6-(4-fluorophenyl)nicotinate (390 mg) and aqueous sodium hydroxide solution (1N, 5.00 ml) and the reaction mixture was treated to afford the title compound (345 mg) as a pale yellow solid.
Workup
- additionthe reaction mixture was treated
Sources & evidence
- ORD record
- ord-e68c8e300c7a42e58d9cf95081c2c404
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06528525B1
Reaction notes
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