Reaktion #1973958

ord-01059e9b86824bd8a8897fc479b50428

Reaktionsgleichung

Nc1ccc(Br)cc1
4-bromoaniline
c1ccncc1
pyridine
CO/C=C/C(=O)Cl
(E)-3-methoxyacryloyl chloride
CO/C=C/C(=O)Nc1ccc(Br)cc1
title compound
Ausbeute 96.0%
CO/C=C/C(=O)Nc1ccc(Br)cc1
(E)-N-(4-bromophenyl)-3-methoxyacrylamide
Ausbeute 96.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe resulting yellow solid was filtered off
  2. 2
    Waschenwashed with water
  3. 3
    SonstigeThe solid was dried under vacuum

Vorschrift

Combined 4-bromoaniline (285 mg, 1.659 mmol), CH2Cl2 (2.0 ml) and pyridine (0.25 ml, 3.09 mmol) and slowly added (E)-3-methoxyacryloyl chloride (200 mg, 1.659 mmol) and stirred at room temperature for 2 h. The resulting yellow solid was filtered off and washed with water. The solid was dried under vacuum to give the title compound (406 mg, 96%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08501238B2uspto-grants-2013_08