Hydrochloric Acid → HCID 4241808, compound
Reaction equation
C([O:3][C:4](=[O:18])[C:5]1[CH:10]=[CH:9][C:8]([N:11]2[CH:16]=[CH:15][C:14](=[O:17])[CH:13]=[CH:12]2)=[CH:7][CH:6]=1)C.[OH-].[K+].Cl>CO>[O:17]=[C:14]1[CH:13]=[CH:12][N:11]([C:8]2[CH:9]=[CH:10][C:5]([C:4]([OH:18])=[O:3])=[CH:6][CH:7]=2)[CH:16]=[CH:15]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 4-(4-oxo-4H-pyridin-1-yl)benzoic acid ethyl ester (10.0 gm, 41.1 mmol), potassium hydroxide (6.92 g, 123 mmol) and methanol (250 ml) was stirred overnight at room temperature. The mixture was acidified by dropwise addition of concentrated hydrochloric acid and the precipitate was collected by suction filtration to give the product as a white powder (9.08 g).
Workup
- filtrationthe precipitate was collected by suction filtration
Sources & evidence
- ORD record
- ord-1a3dd09fceed4ba6a4987fbf665a4fe8
- Source dataset
- uspto-grants-1998_07
- Patent number
- US05783114
Reaction notes
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