Dimethylformamide → Ethyl 4-[2-(1,2,3,4-Tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-7-yl)ethoxy]benzoate
反応式
I[CH2:2][CH2:3][CH:4]1[CH2:10][CH2:9][C:8]2[C:11]([O:21][CH3:22])=[C:12]([O:19][CH3:20])[C:13]([O:17][CH3:18])=[C:14]([O:15][CH3:16])[C:7]=2[CH2:6][CH2:5]1.[OH:23][C:24]1[CH:32]=[CH:31][C:27]([C:28]([O-])=[O:29])=[CH:26][CH:25]=1.[C:33](=O)([O-])[O-].[K+].[K+].CN([CH:42]=[O:43])C>O>[CH3:16][O:15][C:14]1[C:7]2[CH2:6][CH2:5][CH:4]([CH2:3][CH2:2][O:23][C:24]3[CH:32]=[CH:31][C:27]([C:28]([O:43][CH2:42][CH3:33])=[O:29])=[CH:26][CH:25]=3)[CH2:10][CH2:9][C:8]=2[C:11]([O:21][CH3:22])=[C:12]([O:19][CH3:20])[C:13]=1[O:17][CH3:18]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
The mixture of 7-(2-iodoethyl)-1,2,3,4-tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cycloheptene (1.00 g), 4-hydroxybenzoate (593 mg), potassium carbonate (987 mg), and DMF (10 ml) was stirred at room temperature for 12 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride, and dried. The solvent was removed in vacuo. The residue was purified by alumina column chromatography (hexane to hexane:ethyl acetate=15:1) and then with recrystallization from hexane-ethyl acetate to yield the entitled compound (910 mg) as crystals.
後処理
- extractionextracted with ethyl acetate
- washThe organic layer was washed with water and saturated aqueous sodium chloride
- customdried
- customThe solvent was removed in vacuo
- customThe residue was purified by alumina column chromatography (hexane to hexane:ethyl acetate=15:1)
- customwith recrystallization from hexane-ethyl acetate
出典と根拠
- ORDレコード
- ord-4d4276f4cfb847e8a1a206fcd8a0ed35
- 出典データセット
- uspto-grants-2001_12
- 特許番号
- US06326369B1
反応ノート
読み込み中…