Ethanol → 2,2-Dimethylcyclopentanone
反応式
Cl.[NH2:2]O.[C:4]1([CH3:14])[CH:9]=[CH:8][C:7](S(Cl)(=O)=O)=[CH:6][CH:5]=1.[CH3:15][CH2:16][OH:17]>CN(C1C=CN=CC=1)C>[CH3:14][C:4]1([CH3:5])[CH2:9][CH2:8][CH2:7][C:6]1=[O:17].[CH3:5][C:4]1([CH3:14])[NH:2][C:16](=[O:17])[CH2:15][CH2:8][CH2:9]1参加物
6
実験手順
The oxime of 2,2 dimethylcyclopentanone is prepared by reaction of the ketone with hydroxylamine hydrochloride in EtOH, and treated with p-toluenesulfonyl chloride and DMAP. Heating then effects Beckmann rearrangement to give 6,6-dimethyl-2-piperidinone which is deprotonated with NaH in DMF solution. Reaction with n-butyl iodide then gives the title compound.
後処理
- temperatureHeating
出典と根拠
- ORDレコード
- ord-a010d9c3c9ea409e9b454f9466a6ce01
- 出典データセット
- uspto-grants-1991_03
- 特許番号
- US05001113
反応ノート
読み込み中…