Reacción #2383797

ord-05754b3b40ac434bbf4a6729770dc1ff

Ecuación de reacción

CC(C)N(CCO)Cc1cc([N+](=O)[O-])ccc1F
2-[(2-fluoro-5-nitrobenzyl)(isopropyl)amino]ethanol
[Na+].[OH-]
sodium hydroxide
CC(C)N1CCOc2ccc([N+](=O)[O-])cc2C1
4-Isopropyl-7-nitro-2,3,4,5-tetrahydro-1,4-benzoxazepine

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónthe solids were collected by filtration
  2. 2
    ExtracciónThe filtrate was extracted with methylene chloride (3×150 ml)
  3. 3
    Lavadowashed with water
  4. 4
    Secadodried with magnesium sulfate
  5. 5
    Filtraciónfiltered
  6. 6
    Concentraciónconcentrated to an oil
  7. 7
    workup.DISSOLUTIONThe solid and the oil were dissolved in hot 95% ethanol
  8. 8
    Temperaturacooled
  9. 9
    FiltraciónThe solids were collected by filtration (17.47 g, 68%), MS m/z 237 [M+H]+

Procedimiento

To 2-[(2-fluoro-5-nitrobenzyl)(isopropyl)amino]ethanol (31.2 g, 90 mmol) in DMSO (250 ml) was added 25% sodium hydroxide solution (43.2 g, 270 mmol) and the mixture was allowed to stir for 3 h. The reaction was diluted to twice its volume with water and the solids were collected by filtration. The filtrate was extracted with methylene chloride (3×150 ml), washed with water, dried with magnesium sulfate, filtered, and concentrated to an oil. The solid and the oil were dissolved in hot 95% ethanol, then cooled. The solids were collected by filtration (17.47 g, 68%), MS m/z 237 [M+H]+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06489322B1uspto-grants-2002_12