Réaction #51762

ord-233cc62428524c4396e8779a88af5ae1

Équation de réaction

BrBr
bromine
CC(C)c1ccc([N+](=O)[O-])c(N)c1
5-isopropyl-2-nitro-phenylamine
N#C[S-].[Na+]
sodium thiocyanate
[Br-].[Na+]
sodium bromide
CC(C)c1cc(N)c([N+](=O)[O-])cc1SC#N
title compound
CC(C)c1cc(N)c([N+](=O)[O-])cc1SC#N
5-Isopropyl-2-nitro-4-thiocyanato-phenylamine

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    AutreThe crude reaction mixture
  2. 2
    Autrewas purified by flash silica gel chromatography (5%-50% EtOAc in hexanes as eluents)

Mode opératoire

The title compound was prepared according to General Method 13 using 5-isopropyl-2-nitro-phenylamine (prepared in Example PP-1; 5.4 g, 30 mmol), sodium thiocyanate (14.6 g, 180 mmol), sodium bromide (3.7 g, 35.99 mmol), bromine (5.75 g, 36.0 mmol), and MeOH (100 mL). The crude reaction mixture was purified by flash silica gel chromatography (5%-50% EtOAc in hexanes as eluents). MS(APCI): 238 (M+H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US06852711B2uspto-grants-2005_02