反応 #1973963

ord-0b5f5a0d56e74378a80d22d94e83f8bb

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    濃縮Mixture was concentrated under vacuum

実験手順

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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08501238B2uspto-grants-2013_08