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 1 N 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-7182da91e9c24913b03d4f9687516926
- Source dataset
- uspto-grants-1982_10
- Patent number
- US04355033
Reaction notes
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