Hydrochloric Acid → HCID 178489711, compound
Reaction equation
C([O:3][C:4]([C:6]1[NH:10][N:9]=[C:8]([CH:11]=[CH:12][C:13]2[CH:18]=[CH:17][C:16]([OH:19])=[C:15]([O:20][CH3:21])[CH:14]=2)[CH:7]=1)=[O:5])C.[OH-].[K+].Cl>CCO.O>[CH3:21][O:20][C:15]1[CH:14]=[C:13]([CH:12]=[CH:11][C:8]2[CH:7]=[C:6]([C:4]([OH:5])=[O:3])[NH:10][N:9]=2)[CH:18]=[CH:17][C:16]=1[OH:19]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
Ethyl-3-[β-(3-methoxy-4-hydroxyphenyl)ethenyl]-1H-pyrazole-5-carboxylate (0.49 g, 1.7 mmoles) is added to a solution of KOH (0.38 g, 6.8 mmoles) in 0 ml EtOH. The reaction is warmed to reflux overnight. After cooling to room temperature, the reaction is diluted to 200 ml with H2O, and acidified to pH=4 with HCl. A white precipitate forms, and it is collected by filtration. Drying in vacuum in the presence of P2O5 gives 0.3 g (68%) of the desired product, mp=270°-271° C. (dec).
Workup
- temperatureThe reaction is warmed
- temperatureto reflux overnight
- filtrationA white precipitate forms, and it is collected by filtration
- dry with materialDrying in vacuum in the presence of P2O5
Sources & evidence
- ORD record
- ord-a01e9a6cdae64730b1a8c1d842def00d
- Source dataset
- uspto-grants-1993_05
- Patent number
- US05208251
Reaction notes
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