反応式
N1([CH:6]2[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]2)CCCC1.[CH2:12](Cl)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[OH2:20]>O1CCOCC1>[C:13]1([CH2:12][CH:6]2[CH2:7][CH2:8][CH2:9][CH2:10][C:11]2=[O:20])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1参加物
5
実験手順
A mixture of 1-(1-pyrrolidinyl)cyclohexane (85.4 g) and benzyl chloride (100 ml) in dioxane (400 ml) was heated under reflux for 23 hours under nitrogen. Water (100 ml) was then added and the brown oil was distilled to give (2RS)-2-phenylmethylcyclohexanone (47.1 g).
後処理
- temperaturewas heated
- temperatureunder reflux for 23 hours under nitrogen
- distillationthe brown oil was distilled
出典と根拠
- ORDレコード
- ord-21da1710588a4bcabd47799acedec4b2
- 出典データセット
- uspto-grants-1991_10
- 特許番号
- US05057513
関連ノート
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