Reaktion #1008

ord-2a0bdad4b0df4772b53e846d39972e90

Reaktionsgleichung

COc1ccncc1[N+](=O)[O-]
4-Methoxy-3-nitropyridine
CN
methylamine
CNc1ccncc1[N+](=O)[O-]
4-methylamino-3-nitropyridine
Ausbeute 88.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
140°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe bomb was sealed
  2. 2
    Sonstigelowered into an oil bath at 120° C
  3. 3
    Sonstigefell to 90° C.
  4. 4
    Sonstigefor 2 hours
  5. 5
    Sonstige(not very soluble) and the solvent was evaporated

Vorschrift

4-Methoxy-3-nitropyridine (8.17 g, 53.0 mmol) was transferred to a bomb in EtOH (5-10 mL). To this was added a solution of methylamine in EtOH (26.4 mL, 8.03M, 0.212 mol). The bomb was sealed and lowered into an oil bath at 120° C. The bath temperature fell to 90° C. and remained that way for 2 hours. The temperature was raised to 140° C. over 0.5 hour and held there 0.5 hour. The contents were transferred to a flask with EtOH (not very soluble) and the solvent was evaporated. Flash chromatography on silica gel with a gradient of CH2Cl2 /CH3OH gave 7.17 g (88%) of 4-methylamino-3-nitropyridine as a yellow solid: mp 155°-158° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723468uspto-grants-1998_03