Reacción #355750

ord-06ad4cc3d0ec4d17b0de31598f582ee1

Ecuación de reacción

Cc1cc(F)ccc1[N+](=O)[O-]
5-fluoro-2-nitrotoluene
CN1CCCC1=O
N-methylpyrrolidinone
CC(O)CCN
4-amino-2-butanol
CCN(CC)CC
triethylamine
Cc1cc(NCCC(C)O)ccc1[N+](=O)[O-]
4-(4-nitro-3-methylphenylamino)butan-2-ol
Rendimiento 99.6%

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaafter cooling to room temperature
  2. 2
    ExtracciónThe resulting medium was extracted with ethyl acetate
  3. 3
    Concentraciónthe organic phase was then concentrated under vacuum

Procedimiento

2 g of 5-fluoro-2-nitrotoluene were added to a solution of 20 ml of N-methylpyrrolidinone, 1.38 g of 4-amino-2-butanol and 1.57 g of triethylamine. The reaction medium was heated at 60° C. for 10 hours and, after cooling to room temperature, was then poured into a water and ice mixture. The resulting medium was extracted with ethyl acetate and the organic phase was then concentrated under vacuum. 2.88 g of 4-(4-nitro-3-methylphenylamino)butan-2-ol (31) were obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07445645B2uspto-grants-2008_11