Reacción #1973964

ord-c584473cbace4768b1e7d262cf6e1dd2

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe resulting precipitate was filtered
  2. 2
    Otroair-dried

Procedimiento

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%).

Fuente

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