Reaktion #215955
ord-19fe6cc18fd94628b72c94279e7141f8
Reaktionsgleichung
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturheated
- 2Temperaturto reflux for 2 hours
- 3SonstigeThe nitroethane is then evaporated off under reduced pressure
- 4workup.ADDITIONis added
- 5SonstigeAfter separation of the two phases
- 6Waschenthe organic phase is washed with water
- 7TrocknenThe organic phase is then dried over MgSO4
- 8Einengenconcentrated under reduced pressure
- 9Sonstige2.59 g (10.64×10-3 mol) of the expected nitroethylenic compound (yellow solid) are then obtained, equivalent to a 95% yield
Vorschrift
2.13 g (11.20×10-3 mol) of naphthaldehyde, 30 cm3 of nitroethane and 0.54 g (7×10-3 mol) of ammonium acetate are introduced into a round-bottomed flask. The mixture is stirred and heated to reflux for 2 hours. The nitroethane is then evaporated off under reduced pressure, the residue is taken up with CH2Cl2 and water is added to hydrolyze the acetate. After separation of the two phases, the organic phase is washed with water, the aqueous phases with CH2Cl2 (twice). The organic phase is then dried over MgSO4 and concentrated under reduced pressure. 2.59 g (10.64×10-3 mol) of the expected nitroethylenic compound (yellow solid) are then obtained, equivalent to a 95% yield.