Sodium Hydroxide → 2-[3-Methoxy-4-(naphthalen-1-ylmethoxy)-phenyl]-ethylamine
反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][O:8][C:9]1[CH:26]=[C:25]([CH:27]=[CH:28][N+:29]([O-])=O)[CH:24]=[CH:23][C:10]=1[O:11][CH2:12][C:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][CH:14]=1.[OH-].[Na+]>O1CCCC1>[CH3:7][O:8][C:9]1[CH:26]=[C:25]([CH2:27][CH2:28][NH2:29])[CH:24]=[CH:23][C:10]=1[O:11][CH2:12][C:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[CH:16]=[CH:15][CH:14]=1参加物
実験手順
10 g of lithium aluminium hydride are placed in 200 ml of tetrahydrofuran; the mixture is stirred at room temperature. 25.8 g of 1-[2-methoxy-4-(2-nitro-vinyl)-phenoxymethyl]-naphthalene dissolved in 300 ml of tetrahydrofuran are added dropwise thereto over a period of 90 minutes. The reaction mixture is heated at reflux for 4 hours. After cooling, 40 ml of 1 N sodium hydroxide solution are cautiously added dropwise, external cooling being effected using an ice bath. When the addition is complete, the reaction mixture is stirred, without cooling, for one hour, then filtered with suction over Celite and washed with a small amount of tetrahydrofuran. The filtrate is dried over potassium carbonate and concentrated by evaporation, yielding 2-[3-methoxy-4-(naphthalen-1-ylmethoxy)-phenyl]-ethylamine in the form of a brown oil.
後処理
- additionare added dropwise
- temperatureThe reaction mixture is heated
- temperatureat reflux for 4 hours
- temperatureAfter cooling
- temperatureexternal cooling
- additionWhen the addition
- stirringthe reaction mixture is stirred
- temperaturewithout cooling, for one hour
- filtrationfiltered with suction over Celite
- washwashed with a small amount of tetrahydrofuran
- dry with materialThe filtrate is dried over potassium carbonate
- concentrationconcentrated by evaporation
出典と根拠
- ORDレコード
- ord-394898bf230a4a36b0d35ae24f7e562b
- 出典データセット
- uspto-grants-2001_08
- 特許番号
- US06277849B1
反応ノート
読み込み中…