Reacción #2195511

ord-417c23373c1349a998fbed91e20f1f3f

Ecuación de reacción

N#Cc1ccc(CBr)c([N+](=O)[O-])c1
α-bromo-2-nitro-p-tolunitrile
O=C[O-].[Na+]
sodium formate
N#Cc1ccc(CO)c([N+](=O)[O-])c1
title compound
Rendimiento 77.0%
N#Cc1ccc(CO)c([N+](=O)[O-])c1
α-Hydroxy-2-nitro-p-tolunitrile
Rendimiento 77.0%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawas refluxed for 2 h
  2. 2
    Lavadowashed with H2O (3×)
  3. 3
    Secadodried (MgSO4)
  4. 4
    Concentraciónconcentrated
  5. 5
    OtroPurification by flash chromatography (1,2 and 3% MeOH/CHCl3 gradient)

Procedimiento

A stirred solution containing α-bromo-2-nitro-p-tolunitrile (1.228 g, 5.095 mmol) and sodium formate (0.8664 g, 12.74 mmol) in ethanol:water (4:1, 25 mL) was refluxed for 2 h. The reaction was cooled to room temperature, diluted with 20% CH2Cl2/EtOAc, washed with H2O (3×), dried (MgSO4) and concentrated. Purification by flash chromatography (1,2 and 3% MeOH/CHCl3 gradient) gave 0.695 g (77%) of the title compound as a white solid. 1H NMR (DMSO-d6) δ 4.71 (d, 2H), 5.75 (t, 1H), 7.89 (dd, J=7.9 Hz, 1H), 8.14 (d, J=7.9 Hz, 1H), 8.32 (s, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07514411B2uspto-grants-2009_04