反応 #1973958

ord-01059e9b86824bd8a8897fc479b50428

反応方程式

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
収率 96.0%
CO/C=C/C(=O)Nc1ccc(Br)cc1
(E)-N-(4-bromophenyl)-3-methoxyacrylamide
収率 96.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The resulting yellow solid was filtered off
  2. 2
    洗浄washed with water
  3. 3
    その他The solid was dried under vacuum

実験手順

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%).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08501238B2uspto-grants-2013_08