Potassium Hydroxide → 4-Methyl-1H-indole-2-carboxylic acid
Reaction equation
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([C:11]([O:13]C)=[O:12])[NH:6]2.[OH-].[K+]>>[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]2[C:3]=1[CH:4]=[C:5]([C:11]([OH:13])=[O:12])[NH:6]2Participants
3
Procedure
Following the general procedure of PREPARATION 63 and making non-critical variations but starting with methyl 4-methylindole-2-carboxylate (PREPARATION 85, 4.94 g), potassium hydroxide (1.75 g), the title compound is obtained, NMR (300 MHz, CD3OD) 7.24, 7.19, 7.12, 6.85 and 2.51 δ.
Workup
- customthe general procedure of PREPARATION 63
Sources & evidence
- ORD record
- ord-71945745ce3747f09a9f5cee55c29301
- Source dataset
- uspto-grants-1996_02
- Patent number
- US05489593
Reaction notes
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