Реакция #1973964

ord-c584473cbace4768b1e7d262cf6e1dd2

Уравнение реакции

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

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 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%).

Источник

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