反応 #1973965

ord-0c2818d2868d4970981cc7ca88de3e1e

反応方程式

Nc1ccc(Cl)c([N+](=O)[O-])c1
4-chloro-3-nitroaniline
CS(=O)(=O)Cl
methanesulfonyl chloride
c1ccncc1
pyridine
CS(=O)(=O)Nc1ccc(Cl)c([N+](=O)[O-])c1
title compound
収率 92.2%
CS(=O)(=O)Nc1ccc(Cl)c([N+](=O)[O-])c1
N-(4-chloro-3-nitrophenyl)methanesulfonamide
収率 92.2%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The resulting precipitate was filtered
  2. 2
    その他air-dried

実験手順

A mixture of 4-chloro-3-nitroaniline (5.0 g, 29 mmol), methanesulfonyl chloride (2.37 mL, 30.4 mmol) and pyridine (5.9 mL, 72.4 mmol) in THF (100 mL) was stirred for 24 h. Poured in 1M HCl (500 mL). The resulting precipitate was filtered and air-dried to provide the title compound as a solid (6.7 g, 92%).

出典

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