Cyclopentanone → 1-(propan-2-yl)cyclopentanol
反応式
[CH:1]([Mg]Cl)([CH3:3])[CH3:2].[C:6]1(=[O:11])[CH2:10][CH2:9][CH2:8][CH2:7]1>>[CH:1]([C:6]1([OH:11])[CH2:10][CH2:9][CH2:8][CH2:7]1)([CH3:3])[CH3:2]参加物
3
実験手順
According to Example 2, i-PrMgCl (3.30 mL; 3.30 mmol; 1.10 equiv) was reacted with cyclopentanone (252 mg; 3.00 mmol) in the presence of LaCl3.2LiCl (0.33 M; 9.09 mL, 3.00 mmol, 1.00 equiv), the conversion was complete after 5 min (GC monitoring). After workup and careful evaporation of the solvents under reduced pressure, the desired product was obtained as colorless oil (353 mg, 92%). The analytical data were found to be in accordance with the literature data.
後処理
- customAfter workup and careful evaporation of the solvents under reduced pressure
出典と根拠
- ORDレコード
- ord-494c364158d64ef2b3bc6bebef270d5e
- 出典データセット
- uspto-grants-2013_06
- 特許番号
- US08470982B2
反応ノート
読み込み中…