Methyl acetoacetate → E-methyl-5-hydroxy-3-oxo-7-tributylstannyl-6-heptenoate
反応式
[H-].[Na+].[C:3]([O:9][CH3:10])(=[O:8])[CH2:4][C:5]([CH3:7])=[O:6].C([Li])CCC.[CH2:16]([Sn:20]([CH2:29][CH2:30][CH2:31][CH3:32])([CH2:25][CH2:26][CH2:27][CH3:28])/[CH:21]=[CH:22]/[CH:23]=[O:24])[CH2:17][CH2:18][CH3:19]>O1CCCC1.CCCCCC>[CH3:10][O:9][C:3](=[O:8])[CH2:4][C:5](=[O:6])[CH2:7][CH:23]([OH:24])/[CH:22]=[CH:21]/[Sn:20]([CH2:16][CH2:17][CH2:18][CH3:19])([CH2:29][CH2:30][CH2:31][CH3:32])[CH2:25][CH2:26][CH2:27][CH3:28]参加物
反応条件
- 温度
- 0 °C
実験手順
A suspension of sodium hydride (1.28 g) in tetrahydrofuran (70 ml) is cooled to 0° C. and methyl acetoacetate (3.2 ml) added over about 1 minute. The mixture is stirred for about 15 minutes at 0° C., 2.5M n-butyllithium in hexane (12.3 ml) added, stirred for about 20 minutes, E-3-tributylstannylacrolein (10.0 g) in tetrahydrofuran (25 ml) added over five minutes and stirred for about 15 minutes. The mixture is quenched by slow addition of 1M hydrochloric acid, diluted with ether. The aqueous layer is back-extracted with ether and the combined organic solutions washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude product is purified by flash chromatography in 25% ethyl acetate in hexane to give the desired product.
後処理
- stirringstirred for about 20 minutes
- stirringstirred for about 15 minutes
- customThe mixture is quenched by slow addition of 1M hydrochloric acid
- additiondiluted with ether
- extractionThe aqueous layer is back-extracted with ether
- washthe combined organic solutions washed with saturated sodium chloride solution
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe crude product is purified by flash chromatography in 25% ethyl acetate in hexane
出典と根拠
- ORDレコード
- ord-7f72b4dc01b441adafae659ac0bacce6
- 出典データセット
- uspto-grants-1993_06
- 特許番号
- US05216015
反応ノート
読み込み中…