Reaktion #1973965

ord-0c2818d2868d4970981cc7ca88de3e1e

Reaktionsgleichung

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
Ausbeute 92.2%
CS(=O)(=O)Nc1ccc(Cl)c([N+](=O)[O-])c1
N-(4-chloro-3-nitrophenyl)methanesulfonamide
Ausbeute 92.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe resulting precipitate was filtered
  2. 2
    Sonstigeair-dried

Vorschrift

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%).

Quelle

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