Hydroxyamine hydrochloride → HCID 136015764, compound
Reaction equation
[C:1]([C:3](=[N:7][O:8][CH2:9][CH3:10])[C:4](N)=[O:5])#[N:2].C(=O)(O)[O-:12].[Na+].Cl.[NH2:17][OH:18]>O>[C:4]([C:3](=[N:7][O:8][CH2:9][CH3:10])[C:1](=[N:17][OH:18])[NH2:2])([OH:12])=[O:5]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 2-cyano-2-ethoxyimino-acetamide (112.8 g, 0.8 mol) and sodium bicarbonate (134.4 g, 1.6 mol) in water (258 mol), hydroxylamine hydrochloride (61.6 g, 0.88 mol) in water (86 ml) was added dropwise at 80° to 85° C. The mixture was stirred at the same temperature for 3 hrs., and then treated in the same procedure as described in Preparation example 5 to give 2-carboxy-2-ethoxyimino-acetamidoxime (122.5 g) as crystals containing 28.6% of brine. Practical yield: 122.5×0.286=87.5 g. Yield: 62.5%.
Workup
- additionwas added dropwise at 80° to 85° C
- addition, and then treated in the same procedure
- customas described in Preparation example 5
Sources & evidence
- ORD record
- ord-1f8b883166504da3a477a98fdcecd85a
- Source dataset
- uspto-grants-1998_06
- Patent number
- US05773624
Reaction notes
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