Sodium Hydroxide → HCID 23704779, compound
Reaction equation
[CH2:1]([C:3]1[CH:4]=[N:5][C:6]([CH:12]2[NH:16][C:15]([CH:18]([CH3:20])[CH3:19])([CH3:17])[C:14](=[O:21])[NH:13]2)=[C:7]([CH:11]=1)[C:8]([OH:10])=[O:9])[CH3:2].[OH-].[Na+:23]>CO>[CH2:1]([C:3]1[CH:4]=[N:5][C:6]([CH:12]2[NH:16][C:15]([CH:18]([CH3:20])[CH3:19])([CH3:17])[C:14](=[O:21])[NH:13]2)=[C:7]([CH:11]=1)[C:8]([O-:10])=[O:9])[CH3:2].[Na+:23]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To 1.0 g 5-ethyl-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolidinyl)nicotinic acid is added a solution of 0.1498 g sodium hydroxide in 20 mL absolute methanol. The mixture is stirred under nitrogen at room temperature overnight. The solvent is removed to give a solid which is dried in a vacuum oven at 60° C. for two days. The thus-formed sodium 5-ethyl-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolidinyl)nicotinate darkens at 230° C. and decomposes at 247°-250° C.
Workup
- customThe solvent is removed
- customto give a solid which
- customis dried in a vacuum oven at 60° C. for two days
- customdarkens at 230° C.
- customdecomposes at 247°-250° C.
Sources & evidence
- ORD record
- ord-06fe549689b84ba789e71d57c14e8d05
- Source dataset
- uspto-grants-1986_08
- Patent number
- US04608079
Reaction notes
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