Hydroxyamine hydrochloride → HCID 136335088, compound
Reaction equation
[CH2:1]([N:3]1[C:7]([CH:8]=O)=[N:6][CH:5]=[N:4]1)[CH3:2].Cl.[NH2:11][OH:12].C(=O)(O)[O-].[Na+]>C(O)C>[CH2:1]([N:3]1[C:7]([CH:8]=[N:11][OH:12])=[N:6][CH:5]=[N:4]1)[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of crude 1-ethyl-1H-1,2,4-triazole-5-carbaldehyde (17.7 g), hydroxylamine hydrochloride (12.7 g, 0.182 mol), sodium bicarbonate (15.3 g, 0.182 mol) and ethanol (60 mL) was heated at reflux for 3 hours. After cooling, the reaction was filtered and the filtrate concentrated in vacuo. The resulting residue was crystallised from ethanol to give the title compound (6.17 g) 1H-NMR (d6-DMSO) δ 1.32 (3H, t, J=7 Hz), 4.41 (2H, q, J=7 Hz), 8.02 (1H, s), 8.25 (1H, s), 12.70 (1H, s)
Workup
- temperaturewas heated
- temperatureat reflux for 3 hours
- temperatureAfter cooling
- filtrationthe reaction was filtered
- concentrationthe filtrate concentrated in vacuo
- customThe resulting residue was crystallised from ethanol
Sources & evidence
- ORD record
- ord-7571bf433bdc40b49aa7e5a7ec38dfd3
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07446117B2
Reaction notes
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