Iodoethane → HCID 178475109, Verbindung
Reaktionsgleichung
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]([NH:9][OH:10])=[O:8].[H-].[Na+].[CH2:13](I)[CH3:14]>C(O)C>[CH2:13]([O:10][N:9]=[C:7]([C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=1)[OH:8])[CH3:14]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
7 g (0.05 mol) of pyridine-2-hydroxamic acid and 1.4 g (0.05 mol) of sodium hydride were dissolved in 100 ml of ethanol, and 8 g (0.05 mol) of ethyl iodide was gradually dropwise added thereto with stirring. After the dropwise addition, the reaction solution was stirred for 2 hours under reflux condition. After completion of the reaction, the ethanol was distilled off under reduced pressure. To the residue were added suitable amounts of methylene chloride and water, whereby the desired product was extracted with the methylene chloride. The extract was washed with a saturated sodium chloride aqueous solution, and dried over anhydrous sodium sulfate. After the drying, the solvent was distilled off under reduced pressure to obtain 8.2 g of the desired product.
Aufarbeitung
- additionAfter the dropwise addition
- stirringthe reaction solution was stirred for 2 hours
- temperatureunder reflux condition
- customAfter completion of the reaction
- distillationthe ethanol was distilled off under reduced pressure
- additionTo the residue were added suitable amounts of methylene chloride and water, whereby the desired product
- extractionwas extracted with the methylene chloride
- washThe extract was washed with a saturated sodium chloride aqueous solution
- dry with materialdried over anhydrous sodium sulfate
- distillationAfter the drying, the solvent was distilled off under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-f81bbc828061408a8a6798b18b52b41e
- Quelldatensatz
- uspto-grants-1982_04
- Patentnummer
- US04327089
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