Reaktion #2551

ord-1e483b3adf244fe28b89df6ce80d81bc

Reaktionsgleichung

COc1ccccc1NC(=O)c1ccc(CCl)cc1
4-Chloromethyl-N-(2-methoxyphenyl)benzamide
CN
methylamine
CNCc1ccc(C(=O)Nc2ccccc2OC)cc1
title compound
Ausbeute 100.0%
CNCc1ccc(C(=O)Nc2ccccc2OC)cc1
N-(2-Methoxyphenyl)-4-(methylamino)methylbenzamide
Ausbeute 100.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas removed by evaporation
  2. 2
    workup.ADDITIONthe resulting residue was diluted with methylene chloride (10 ml)
  3. 3
    TrocknenAfter drying on anhydrous sodium carbonate
  4. 4
    Sonstigethe solvent was removed by evaporation

Vorschrift

4-Chloromethyl-N-(2-methoxyphenyl)benzamide (400 mg, 1.45 mmol) was dissolved in dioxane (4 ml) and then mixed with 50% methylamine aqueous solution (4 ml) at room temperature. After 1 hour of stirring at the same temperature, dioxane was removed by evaporation, and the resulting residue was diluted with methylene chloride (10 ml). After drying on anhydrous sodium carbonate, the solvent was removed by evaporation to obtain 500 mg (100%) of the title compound in the form of colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728835uspto-grants-1998_03