反応式
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)=[C:6]([CH:11]=1)[C:7]([O:9]C)=[O:8].[ClH:18]>C(O)(=O)C>[ClH:18].[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)=[C:6]([CH:11]=1)[C:7]([OH:9])=[O:8]参加物
4
実験手順
A mixture of methyl 5-methyl-2-(pyridin-4-yl)benzoate (8.8 g), 6 N hydrochloric acid (65 mL) and acetic acid (100 mL) was heated under reflux overnight. The solvent was evaporated under reduced pressure, and the obtained solid was washed with ethyl acetate to give the title compound (6.6 g).
後処理
- temperaturewas heated
- temperatureunder reflux overnight
- customThe solvent was evaporated under reduced pressure
- washthe obtained solid was washed with ethyl acetate
出典と根拠
- ORDレコード
- ord-0a540f8d1f964085a3e8917c705f8f16
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08865717B2
関連ノート
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