Reaction #1973963

ord-0b5f5a0d56e74378a80d22d94e83f8bb

Reaction equation

Nc1ccc([N+](=O)[O-])c([N+](=O)[O-])c1
3,4-dinitroaniline
CS(=O)(=O)Cl
methanesulfonyl chloride
c1ccncc1
pyridine
CS(=O)(=O)Nc1ccc([N+](=O)[O-])c([N+](=O)[O-])c1
title compound
CS(=O)(=O)Nc1ccc([N+](=O)[O-])c([N+](=O)[O-])c1
N-(3,4-dinitrophenyl)methanesulfonamide

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    ConcentrationMixture was concentrated under vacuum

Procedure

A mixture of 3,4-dinitroaniline (5.27 g, 28.8 mmol), methanesulfonyl chloride (3.36 mL, 43.1 mmol) and pyridine (5.82 mL, 71.9 mmol) in CH2Cl2 (100 mL) was stirred for 24 h. Mixture was concentrated under vacuum to provide a crude semi-solid title compound that was used without further purification.

Source

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