Hydrochloric Acid → 8-Ethyl-2-methylquinoline-4-carboxylic acid
Reaction equation
C([O:3][C:4]([C:6]1[C:15]2[C:10](=[C:11]([CH2:16][CH3:17])[CH:12]=[CH:13][CH:14]=2)[N:9]=[C:8]([CH3:18])[CH:7]=1)=[O:5])C.Cl>>[CH2:16]([C:11]1[CH:12]=[CH:13][CH:14]=[C:15]2[C:10]=1[N:9]=[C:8]([CH3:18])[CH:7]=[C:6]2[C:4]([OH:5])=[O:3])[CH3:17]Participants
3
Procedure
8-Ethyl-2-methylquinoline-4-carboxylic acid ethyl ester (0.205 g) and 5N HCl combined and the solution boiled for 7 h. Solvent was removed at reduced pressure to give the title compound (0.195 g) as a yellow solid. m/z (API+): 216 (MH+), 214 (API−) 214(M-H).
Workup
- customSolvent was removed at reduced pressure
Sources & evidence
- ORD record
- ord-c7903352670b44bdb4f7dc4e9dea4401
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06699879B1
Reaction notes
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