Sodium Hydroxide → HCID 178526276, compound
Reaction equation
Br.[Cl:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([Cl:9])[C:4]=1[N:10]=[C:11]1[NH:15][CH2:14][CH2:13][N:12]1[OH:16].[OH-].[Na+]>O>[Cl:9][C:5]1[CH:6]=[CH:7][CH:8]=[C:3]([Cl:2])[C:4]=1[N:10]=[C:11]1[NH:15][CH2:14][CH2:13][N:12]1[OH:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.6 g. of 2-[(2,6-dichlorophenyl)imino]-1-hydroxyimidazolidine hydrobromide is dissolved in a little water and the pH is adjusted to 10 with 1N caustic soda solution. The precipitate formed is extracted with methylene chloride. The organic extracts are dried over sodium sulfate and evaporated to dryness. The residue is recrystallized from acetonitrile, whereupon 2-[(2,6-dichlorophenyl)imino]-1-hydroxyimidazolidine, m.p. 215° (decomp.) is obtained.
Workup
- customThe precipitate formed
- extractionis extracted with methylene chloride
- dry with materialThe organic extracts are dried over sodium sulfate
- customevaporated to dryness
- customThe residue is recrystallized from acetonitrile, whereupon 2-[(2,6-dichlorophenyl)imino]-1-hydroxyimidazolidine
- customm.p. 215° (decomp.) is obtained
Sources & evidence
- ORD record
- ord-1d15964473974054a3251c4a867305fd
- Source dataset
- uspto-grants-1985_04
- Patent number
- US04511720
Reaction notes
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