Lithium hydroxide, monohydrate → 3-Methoxyindole-6-carboxylic acid
Reaction equation
C([N:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([C:13]([O:15]C)=[O:14])[CH:11]=2)[C:6]([O:17][CH3:18])=[CH:5]1)(=O)C.O.[OH-].[Li+]>C1COCC1.O>[CH3:18][O:17][C:6]1[C:7]2[C:12](=[CH:11][C:10]([C:13]([OH:15])=[O:14])=[CH:9][CH:8]=2)[NH:4][CH:5]=1Participants
5
Conditions
- Temperature
- 50 °C
Procedure
To a solution of methyl 1-acetyl-3-methoxyindole-6-carboxylate (74 mg, 0.3 mmol) in THF (10 ml) and water (2 ml) was added lithium hydroxide hydrate (63 mg, 1.5 mmol). The reaction mixture was warmed to 50° C. and stirred for 3 h. The THF was removed under reduced pressure and the pH of the aqueous phase adjusted to 3. Extraction of the aqueous layer with ethyl acetate, drying and concentration gave the acid (50 mg, 87%);
Workup
- customThe THF was removed under reduced pressure
- extractionExtraction of the aqueous layer with ethyl acetate
- customdrying
- concentrationconcentration
Sources & evidence
- ORD record
- ord-a114a88948d74f7f916aad27722aebe7
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06855715B1
Reaction notes
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