Nitric Acid → 9-Bromononanoic Acid
Reaktionsgleichung
[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][OH:11].[N+]([O-])(O)=[O:13]>>[Br:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C:10]([OH:13])=[O:11]Komponenten
3
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
9-Bromo-1-nonanol (4 g, 18 mmol) was placed in a flask, cooled on an ice bath, and concentrated nitric acid (40 mL) was slowly added. The solution was stirred at 0° C. for 30 minutes then allowed to warm to room temperature and stirring continued overnight. The solution was poured onto ice and extracted with DCM (3×150 mL). The combined extracts were washed with water (3×150 mL) and the solvent then removed in vacuo to give an oil 3.82 g (94%);
Aufarbeitung
- temperaturecooled on an ice bath
- temperatureto warm to room temperature
- stirringstirring continued overnight
- additionThe solution was poured onto ice
- extractionextracted with DCM (3×150 mL)
- washThe combined extracts were washed with water (3×150 mL)
- customthe solvent then removed in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-6b95dc8a398840299e15ff37546ae144
- Quelldatensatz
- uspto-grants-1997_03
- Patentnummer
- US05610145
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