Reaktion #67577
ord-72f590626e554352bf116ca47a992441
Reaktionsgleichung
2-Bromopyridine
methylhydrazine
methylhydrazine
→
N-Methyl-N-pyridin-2-yl-hydrazine
Ausbeute 74.4%
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigefitted with a water-condenser
- 2SonstigeAfter a few minutes a vigorous exothermic reaction
- 3Sonstigethe excess methylhydrazine was removed under reduced pressure
- 4Extraktionthe resulting solution was extracted with ether (3×100 ml)
- 5TrocknenThe combined extracts were dried (K2CO3)
- 6Sonstigepurified by silica gel chromatography 0-3% EtOH/CH2Cl2
Vorschrift
2-Bromopyridine (5 mL, 52.4 mmol) and methylhydrazine (20 mL, 360 mmol) were mixed together in a flask fitted with a water-condenser. After a few minutes a vigorous exothermic reaction occurred with refluxing of the methylhydrazine. When the reaction had subsided, the mixture was left for 16 hours, and the excess methylhydrazine was removed under reduced pressure. The cooled residue was stirred with aqueous sodium hydroxide solution (30 ml of 20%), and the resulting solution was extracted with ether (3×100 ml). The combined extracts were dried (K2CO3) and purified by silica gel chromatography 0-3% EtOH/CH2Cl2 to give 4.8 g of N-Methyl-N-pyridin-2-yl-hydrazine.