Reaktion #67577

ord-72f590626e554352bf116ca47a992441

Reaktionsgleichung

Brc1ccccn1
2-Bromopyridine
CNN
methylhydrazine
CNN
methylhydrazine
CN(N)c1ccccn1
N-Methyl-N-pyridin-2-yl-hydrazine
Ausbeute 74.4%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigefitted with a water-condenser
  2. 2
    SonstigeAfter a few minutes a vigorous exothermic reaction
  3. 3
    Sonstigethe excess methylhydrazine was removed under reduced pressure
  4. 4
    Extraktionthe resulting solution was extracted with ether (3×100 ml)
  5. 5
    TrocknenThe combined extracts were dried (K2CO3)
  6. 6
    Sonstigepurified 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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08524764B2uspto-grants-2013_09