Reacción #1973963

ord-0b5f5a0d56e74378a80d22d94e83f8bb

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    ConcentraciónMixture was concentrated under vacuum

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08501238B2uspto-grants-2013_08