Sodium Hydroxide → HCID 23673134, compound
Reaction equation
[OH-].[Na+:2].[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[N:11]([CH3:23])[C:12]([CH2:20][CH2:21][CH3:22])=[C:13]([C:17](=[O:19])[CH:18]=2)[C:14]([OH:16])=[O:15])=[CH:6][CH:5]=1>CO>[Cl:3][C:4]1[CH:5]=[CH:6][C:7]([C:10]2[N:11]([CH3:23])[C:12]([CH2:20][CH2:21][CH3:22])=[C:13]([C:17](=[O:19])[CH:18]=2)[C:14]([O-:16])=[O:15])=[CH:8][CH:9]=1.[Na+:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.42 g (0.0052 mol) of 50% aqueous sodium hydroxide is added to a suspension of 1.6 g (0.0052 mol) 6-(4-chlorophenyl)-1-methyl-2-n-propyl-4-oxonicotinic acid in 25 ml of methanol. The solution formed is allowed to stand at room temperature for 1 hr. and is concentrated in vacuo. The concentrate is dried to afford 1.5 g (88% yield) of product.
Workup
- customThe solution formed
- concentrationand is concentrated in vacuo
- customThe concentrate is dried
Sources & evidence
- ORD record
- ord-ea9e5882477940f3928c4fcb6dfe63ee
- Source dataset
- uspto-grants-1990_06
- Patent number
- US04936904
Reaction notes
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