Potassium Hydroxide → 2-(6-Methoxypyridin-2-yl)-2-methylpropanoic acid
Reaction equation
C([O:3][C:4](=[O:16])[C:5]([C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([O:14][CH3:15])[N:9]=1)([CH3:7])[CH3:6])C.[OH-].[K+]>CO>[CH3:15][O:14][C:10]1[N:9]=[C:8]([C:5]([CH3:7])([CH3:6])[C:4]([OH:16])=[O:3])[CH:13]=[CH:12][CH:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2-(6-Methoxy-pyridin-2-yl)-2-methyl-propionic acid ethyl ester (5.33 g) was dissolved in methanol (200 ml), added with 5 N aqueous solution of potassium hydroxide (25 ml), and then stirred under reflux. The reaction mixture was concentrated and neutralized with 2 N hydrochloric acid. The precipitated matters were collected by filtration and dried to obtain the title compound (3.55 g).
Workup
- temperatureunder reflux
- concentrationThe reaction mixture was concentrated
- filtrationThe precipitated matters were collected by filtration
- customdried
Sources & evidence
- ORD record
- ord-68ac0fb7778f4719bde87654e031adc3
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09440922B2
Reaction notes
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