Reaktion #5099

ord-7a603da7931848aeaaadbcc3c883c330

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe solvent was removed by evaporation under a reduced pressure
  2. 2
    Sonstigeto the residue thus obtained
  3. 3
    Temperaturcooled
  4. 4
    Sonstigecrystallized
  5. 5
    FiltrationThe crystals were collected by filtration
  6. 6
    Waschenwashed with water
  7. 7
    Sonstigerecrystallized from water

Vorschrift

200 Grams of 6-chloroacetylaminomethyl-2,3-dihydro-7-hydroxy-4-methyl-1H-indene-1-one, 77.9 g of hydroxylamine hydrochloride, 300 ml of pyridine and 1,800 ml of ethanol were refluxed for 3 hours. After the reaction was completed, the solvent was removed by evaporation under a reduced pressure, then to the residue thus obtained was added 2 liters of water and the mixture was stirred vigorously, cooled and crystallized. The crystals were collected by filtration, washed with water, and recrystallized from water to obtain 167 g of (2,3-dihydro-7-hydroxy-1-hydroxyimino-4-methyl-1H-indene-6yl)-methylaminocarbonylmethylpyridinium chloride. Colorless flake-like crystals. Melting point: 279° C. (Decomposed).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05242919uspto-grants-1993_09