反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]2[CH2:7][C:8]3[CH:14]=[C:13]([CH:15]([CH3:19])[C:16]([OH:18])=[O:17])[CH:12]=[CH:11][C:9]=3[O:10][C:2]=12.CC(C)[O-].[Al+3:24].CC(C)[O-].CC(C)[O-].O>C(O)(C)C>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]2[CH2:7][C:8]3[CH:14]=[C:13]([CH:15]([CH3:19])[C:16]([O-:18])=[O:17])[CH:12]=[CH:11][C:9]=3[O:10][C:2]=12.[Al+3:24].[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]2[CH2:7][C:8]3[CH:14]=[C:13]([CH:15]([CH3:19])[C:16]([O-:18])=[O:17])[CH:12]=[CH:11][C:9]=3[O:10][C:2]=12.[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]2[CH2:7][C:8]3[CH:14]=[C:13]([CH:15]([CH3:19])[C:16]([O-:18])=[O:17])[CH:12]=[CH:11][C:9]=3[O:10][C:2]=12参加物
5
実験手順
2.5 G of 2-(5H-[1]benzopyrano[2,3-b]pyridin-7-yl)propionic acid is dissolved in 80 ml of isopropyl alcohol. A solution of 2.1 g of aluminum isopropoxide in 25 ml of isopropyl alcohol is added dropwise to the solution with stirring, white crystals being immediately yielded. After refluxing the mixture for 1 hour, 3 ml of water is added, and then the whole mixture is further refluxed for 1 hour. After cooling, the crystals are filtered off, washed with isopropyl alcohol, and dried to give aluminum 2-(5H-[1]-benzopyrano[2,3-b]pyridin-7-yl)propionate as white crystals melting at above 250°C.
後処理
- customwhite crystals being immediately yielded
- temperatureAfter refluxing the mixture for 1 hour
- temperaturethe whole mixture is further refluxed for 1 hour
- temperatureAfter cooling
- filtrationthe crystals are filtered off
- washwashed with isopropyl alcohol
- customdried
出典と根拠
- ORDレコード
- ord-046c44be7a3645999781925f225f62a5
- 出典データセット
- uspto-grants-1976_01
- 特許番号
- US03931205
関連ノート
読み込み中…