Lithium Hydroxide → 6-Bromo-3-hydroxypyridine-2-carboxylic acid
Reaction equation
[Br:1][C:2]1[N:7]=[C:6]([C:8]([O:10]C)=[O:9])[C:5]([OH:12])=[CH:4][CH:3]=1.[Li+].[OH-]>CO>[Br:1][C:2]1[N:7]=[C:6]([C:8]([OH:10])=[O:9])[C:5]([OH:12])=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Methyl 6-bromo-3-hydroxypicolinate (26B) (464 mg, 2 mmol) in MeOH (0.5 mL) was added to a solution of LiOH (200 mg in 2 mL water). The reaction mixture was stirred at rt for 2 h. The product precipitated out of solution and was filtered, washed with water, and dried under reduced pressure to provide the desired product 6-bromo-3-hydroxypicolinic acid (55A). 1H NMR (300 MHz, CDCl3): 7.6 (1H, d), 7.32 (1H, d).
Workup
- customThe product precipitated out of solution
- filtrationwas filtered
- washwashed with water
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-0478866daf2e40c2a8d3499ebf053e21
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08518970B2
Reaction notes
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