Reaktion #725654
ord-104cf1dd1c7049108a3563153a7a8e8e
Reaktionsgleichung
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturthen cooled to room temperature
- 2SonstigeThe organic layer separated
- 3Waschenwashed with a saturated sodium chloride solution (3×75 mL)
- 4TrocknenAfter drying over magnesium sulfate
- 5Filtrationfiltering
- 6workup.DISTILLATIONdistilled (0.5 Torr, 36° C.) which
- 7Sonstigeremoved unreacted 1-dodecene
- 8workup.ADDITIONcontaining 1-nitro-2-dodecene and 1-nitro-2-dodecanol
- 9SonstigeThis oil was further reacted with methanesulfonyl chloride and triethylamine
Vorschrift
1-Dodecene (222 mL, 1.0 mole) and concentrated nitric acid (96 mL, 1.5 moles) were mixed together at room temperature. The solution was heated to 100° C. for 4 hours with rapid stirring then cooled to room temperature. The organic layer separated and washed with a saturated sodium chloride solution (3×75 mL). After drying over magnesium sulfate and filtering, the orange oil was vacuum distilled (0.5 Torr, 36° C.) which removed unreacted 1-dodecene. The remaining orange/red oil is a mixture containing 1-nitro-2-dodecene and 1-nitro-2-dodecanol. This oil was further reacted with methanesulfonyl chloride and triethylamine to dehydrate the alcohol and produce more 1-nitro-2-dodecene. After this dehydration step, the structure of 1-nitro-2-dodecene was confirmed by IR and GC analysis.