Reaction #1973965

ord-0c2818d2868d4970981cc7ca88de3e1e

Reaction equation

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

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

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

Procedure

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%).

Source

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