Pyridine → 4-Dimethylaminocyclohexanone oxime
反応式
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]1参加物
実験手順
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.
後処理
- temperatureheated
- temperatureat reflux for 30 minutes
- customThe resulting crystalline solid was collected
- washwashed with cold ethanol
- dissolutionThe solid was then dissolved in water
- additionby the addition of potassium carbonate
- extractionThe aqueous phase was then extracted with dichloromethane which
- dry with materialdried over sodium sulfate
- concentrationconcentrated under reduced pressure
- customto provide a crystalline solid
- customThis solid was recrystallized from ethanol
出典と根拠
- ORDレコード
- ord-469497bbaac74cc59738d03f1b53b70a
- 出典データセット
- uspto-grants-1998_12
- 特許番号
- US05846995
反応ノート
読み込み中…