Nitroethane → HCID 54097466, compound
Reaction equation
[CH2:1]([O:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH:13]=O)=[CH:9][N:8]=1)[CH3:2].[N+:15]([CH2:18][CH3:19])([O-:17])=[O:16].C([O-])(=O)C.[NH4+]>C(O)(=O)C.O>[CH2:1]([O:3][CH2:4][CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH:13]=[C:18]([N+:15]([O-:17])=[O:16])[CH3:19])=[CH:9][N:8]=1)[CH3:2]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 8.3 g (42.6 mmol) of 2-(2-ethoxyethoxy)-pyridine-5-aldehyde, 5.53 g, (73.7 mmol) of nitroethane and 3.83 g (49.7 mmol) of ammonium acetate in 50 ml of glacial acetic acid is heated under reflux for 7 hours. The mixture is then diluted with water while cooling in ice, and the product is filtered off with suction.
Workup
- temperatureis heated
- temperatureunder reflux for 7 hours
- temperaturewhile cooling in ice
- filtrationthe product is filtered off with suction
Sources & evidence
- ORD record
- ord-c1fb0774bcfe408d931b24205163cee3
- Source dataset
- uspto-grants-1993_06
- Patent number
- US05216170
Reaction notes
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