(5S)-4-[(4-Methoxyphenyl)methyl]-5-methylmorpholin-3-one → HCID 59525840、化合物
反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][O:8][C:9]1[CH:23]=[CH:22][C:12]([CH2:13][N:14]2[C@@H:19]([CH3:20])[CH2:18][O:17][CH2:16][C:15]2=O)=[CH:11][CH:10]=1>C1COCC1>[CH3:7][O:8][C:9]1[CH:10]=[CH:11][C:12]([CH2:13][N:14]2[CH2:15][CH2:16][O:17][CH2:18][C@@H:19]2[CH3:20])=[CH:22][CH:23]=1参加物
反応条件
- 温度
- 0 °C
実験手順
Into a 5000 mL 4-necked, round bottomed flask purged and maintained with an inert atmosphere of nitrogen was placed a suspension of lithium aluminum hydride (60.04 g, 1.58 mol) in THF (2000 mL), followed by the dropwise addition of a solution of (S)-4-(4-methoxybenzyl)-5-methylmorpholin-3-one (186 g, 790.48 mmol) in THF (300 mL). The resulting solution was heated to reflux for 1 hour. The reaction mixture was cooled to 0° C., quenched by adding 500 mL of ethyl acetate and then 500 mL of water, the resulting solution was extracted three times with 2000 mL of ethyl acetate. The combined organic layer was dried over MgSO4, filtered, and concentrated under vacuum. The residue was purified by flash chromatography (silica, 1:30 ethyl acetate/petroleum ether) to afford the title compound as a yellow oil.
後処理
- customInto a 5000 mL 4-necked, round bottomed flask purged
- temperaturemaintained with an inert atmosphere of nitrogen
- temperatureThe resulting solution was heated
- temperatureto reflux for 1 hour
- customquenched
- additionby adding 500 mL of ethyl acetate
- extraction500 mL of water, the resulting solution was extracted three times with 2000 mL of ethyl acetate
- dry with materialThe combined organic layer was dried over MgSO4
- filtrationfiltered
- concentrationconcentrated under vacuum
- customThe residue was purified by flash chromatography (silica, 1:30 ethyl acetate/petroleum ether)
出典と根拠
- ORDレコード
- ord-6365588d1af3408ca3a37fe3b2dce98e
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08367706B2
反応ノート
読み込み中…