Reaktion #1973964

ord-c584473cbace4768b1e7d262cf6e1dd2

Reaktionsgleichung

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
Ausbeute 100.0%
CS(=O)(=O)Nc1ccc([N+](=O)[O-])c(Cl)c1
N-(3-chloro-4-nitrophenyl)methanesulfonamide
Ausbeute 100.0%

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 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%).

Quelle

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