Pyridine → 4-Dimethylaminocyclohexanone oxime

HRID 1457056Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1457056
Cl.[CH3:2][N:3]([CH3:11])[CH:4]1[CH2:9][CH2:8][C:7](=O)[CH2:6][CH2:5]1.Cl.[NH2:13][OH:14].N1C=CC=CC=1>C(O)C>[CH3:2][N:3]([CH3:11])[CH:4]1[CH2:9][CH2:8][C:7](=[N:13][OH:14])[CH2:6][CH2:5]1

Komponenten

5

Versuchsvorschrift

A mixture of 1.78 gm (10 mMol) of 4-dimethylaminocyclohexanone hydrochloride and 0.70 gm (10 mMol) of hydroxylamine hydrochloride in 25 mL ethanol was treated with 3 mL pyridine and then heated at reflux for 30 minutes. The reaction mixture was then cooled to room temperature and stored at 4° C. for 18 hours. The resulting crystalline solid was collected and washed with cold ethanol. The solid was then dissolved in water and the aqueous solution made basic by the addition of potassium carbonate. The aqueous phase was then extracted with dichloromethane which contained a small amount of isopropanol. The organic extracts were combined, dried over sodium sulfate and concentrated under reduced pressure to provide a crystalline solid. This solid was recrystallized from ethanol to provide 1.05 gm (67%) of the desired oxime.

Aufarbeitung

  1. temperatureheated
  2. temperatureat reflux for 30 minutes
  3. customThe resulting crystalline solid was collected
  4. washwashed with cold ethanol
  5. dissolutionThe solid was then dissolved in water
  6. additionby the addition of potassium carbonate
  7. extractionThe aqueous phase was then extracted with dichloromethane which
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated under reduced pressure
  10. customto provide a crystalline solid
  11. customThis solid was recrystallized from ethanol

Quellen und Nachweise

ORD-Eintrag
ord-469497bbaac74cc59738d03f1b53b70a
Quelldatensatz
uspto-grants-1998_12
Patentnummer
US05846995

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