反応式
[CH:1]1[CH:10]=[C:9]([OH:11])[C:8]2[N:7]=CC(O)=[CH:4][C:3]=2[CH:2]=1.[N+](=[CH2:15])=[N-].C[CH2:17][O:18][CH2:19][CH3:20]>C(O)C>[CH3:17][O:18][C:19]1[CH:20]=[N:7][C:8]2[C:3]([CH:4]=1)=[CH:2][CH:1]=[CH:10][C:9]=2[O:11][CH3:15]参加物
4
実験手順
Jineol of 4.5 mg was dissolved in 2 ml of ethanol, and diazomethane ether solution was slowly dropped to the solution. After the excess of diazomethane and solvent was removed by purging with nitrogen gas, the solution was purified by silicagel chromatography to give 4.2 mg of 3,8-dimethoxy quinoline with 80% yield.
後処理
- customAfter the excess of diazomethane and solvent was removed
- customby purging with nitrogen gas
- customthe solution was purified by silicagel chromatography
出典と根拠
- ORDレコード
- ord-a3d35d944aca43608a8e9c356519b602
- 出典データセット
- uspto-grants-1998_10
- 特許番号
- US05824689
関連ノート
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