反応式
[CH3:1][C:2]1[CH2:6][CH:5]=[CH:4][CH:3]=1.[CH3:7][C:8]([CH3:10])=O.N1CCCC1.C(O)(=O)C>CCOCC.O.CO>[CH3:1][C:2]1[CH:6]=[CH:5][C:4](=[C:8]([CH3:10])[CH3:7])[CH:3]=1参加物
8
実験手順
To 130 ml of dehydrated methanol, 22.6 g (283 mmol) of methylcyclopentadiene and 8.50 ml (116 mmol) of acetone were added, then 14.5 ml (174 mmol) of pyrrolidine was dropwise added at 0° C., and the mixture was reacted at room temperature for one night. Then, 10 ml (180 mmol) of acetic acid was added at 0° C. The mixture was diluted with ether and water and then subjected to extraction. Then, the organic phase was separated, washed with water and dried over anhydrous magnesium sulfate to obtain 12.9 g of a brown liquid. The analyzed values are given below.
後処理
- customthe mixture was reacted at room temperature for one night
- extractionsubjected to extraction
- customThen, the organic phase was separated
- washwashed with water
- dry with materialdried over anhydrous magnesium sulfate
出典と根拠
- ORDレコード
- ord-fdbc8625ce7c4974aa93c7c7a2911c2a
- 出典データセット
- uspto-grants-2005_09
- 特許番号
- US06939928B1
関連ノート
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