Реакция #1973965

ord-0c2818d2868d4970981cc7ca88de3e1e

Уравнение реакции

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

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe resulting precipitate was filtered
  2. 2
    Другоеair-dried

Методика

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%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08501238B2uspto-grants-2013_08