Water → 1-(2-Pyridyl)cyclopentene
反応式
O[CH:2]1[CH2:6][CH2:5][CH2:4][CH:3]1[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][N:8]=1.O>C(Cl)Cl>[N:8]1[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=1[C:3]1[CH2:4][CH2:5][CH2:6][CH:2]=1参加物
4
反応条件
- 温度
- 170 °C
実験手順
In an autoclave, 60.0 g (368 mM) of 1-hydroxy-2-(2-pyridyl)cyclopentane was placed and stirred for 60 hours at 170° C., followed by cooling, addition of water and extraction with methylene chloride. The organic layer was dried with anhydrous sodium sulfate, followed by distilling-off of the solvent under reduced pressure and then purification by silica gel column chromatography (eluent: hexane/ethyl acetate=8/1) to obtain 28.0 g of liquid 1-(2-pyridyl)cyclopentene (Yield: 52.5%).
後処理
- temperatureby cooling
- dry with materialThe organic layer was dried with anhydrous sodium sulfate
- custompurification by silica gel column chromatography (eluent: hexane/ethyl acetate=8/1)
出典と根拠
- ORDレコード
- ord-88c005ed4bf74721916cefb4506249f3
- 出典データセット
- uspto-grants-2004_05
- 特許番号
- US06733905B2
反応ノート
読み込み中…