Reacción #709268

ord-86d07e316d734974bf3e4f7bf313c34a

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted twice with 10 ml of chloroform each time
  2. 2
    OtroAfter the chloroform has been evaporated off
  3. 3
    Otrothe residue crystallizes in yellow crystals from a little ethanol

Procedimiento

2 g (4.7 mmol) of 2-methyl-8a-morpholino-3-nitro-4-(2-trifluoromethylphenyl)-4a,5,6,7,8,8a-hexahydro-4H-chromene are suspended in 15 ml of ethanol and dissolved with about 3 ml of concentrated aqueous ammonia solution at 30° to 45° C. The pH is then brought to 3 with concentrated hydrochloric acid and the solution is diluted with 5 ml of water and extracted twice with 10 ml of chloroform each time. After the chloroform has been evaporated off, the residue crystallizes in yellow crystals from a little ethanol.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04769375uspto-grants-1988_09