反応 #1973964

ord-c584473cbace4768b1e7d262cf6e1dd2

反応方程式

Nc1ccc([N+](=O)[O-])c(Cl)c1
3-chloro-4-nitroaniline
CS(=O)(=O)Cl
methanesulfonyl chloride
c1ccncc1
pyridine
CS(=O)(=O)Nc1ccc([N+](=O)[O-])c(Cl)c1
title compound
収率 100.0%
CS(=O)(=O)Nc1ccc([N+](=O)[O-])c(Cl)c1
N-(3-chloro-4-nitrophenyl)methanesulfonamide
収率 100.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

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

実験手順

A mixture of 3-chloro-4-nitroaniline (4.85 g, 28.1 mmol), methanesulfonyl chloride (3.29 mL, 42.2 mmol) and pyridine (6.82 mL, 84 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 (7.03 g, 100%).

出典

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