Hydrochloric Acid → HCID 15067108, compound
Reaction equation
Cl.[CH2:2]([O:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([CH:14]=[C:15]([N+]([O-])=O)[CH3:16])=[CH:10][N:9]=1)[CH3:3].C[OH:21]>[Fe]>[CH2:2]([O:4][CH2:5][CH2:6][O:7][C:8]1[CH:13]=[CH:12][C:11]([CH2:14][C:15](=[O:21])[CH3:16])=[CH:10][N:9]=1)[CH3:3]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
6.5 ml of concentrated hydrochloric acid are added dropwise to a boiling suspension of 800 mg (3.2 mmol) of 1-[2-(2-ethoxyethoxy)-5-pyridyl]-2-nitro-1-propene and 710 mg of iron filings in 10 ml of methanol. After 30 minutes the mixture is filtered and diluted with water. It is washed with ether, adjusted to pH 7 and extracted with ether. The organic phase is washed with 1% strength aqueous sodium hydroxide solution and then with water, dried over sodium sulphate and evaporated.
Workup
- filtrationAfter 30 minutes the mixture is filtered
- additiondiluted with water
- washIt is washed with ether
- extractionextracted with ether
- washThe organic phase is washed with 1% strength aqueous sodium hydroxide solution
- dry with materialwith water, dried over sodium sulphate
- customevaporated
Sources & evidence
- ORD record
- ord-865cb7f1c8764103b8228c54c616bbb7
- Source dataset
- uspto-grants-1991_07
- Patent number
- US05028617
Reaction notes
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