反応式
[C:1](Cl)(=[O:9])[CH:2]([CH2:6][CH2:7][CH3:8])[CH2:3][CH2:4][CH3:5].ICC[OH:14]>>[C:1]([OH:9])(=[O:14])[CH:2]([CH2:6][CH2:7][CH3:8])[CH2:3][CH2:4][CH3:5]参加物
3
反応条件
- 温度
- 100 °C
実験手順
To the product of Example 87 (4.87 g, 30 mmol), 2-iodoethanol (5.16 g, 30 mmol) was added with stirring and cooling in an ice bath. The neat mixture was then heated to 100° C. in a water bath for 10 minutes, then removed from the heat and stirred for an additional 10 minutes. The reaction mixture was then dissolved in 50 ml of ether, washed with water (1×30 ml), 5% NaOH (2×30 ml), and again with water (2×30 ml). The ether layer was dried over anhydrous sodium sulfate and the solvent was removed under reduced pressure. A light yellow liquid product was obtained in 67% yield from valproic acid (6.0 g). Silver nitrate gave a bright yellow precipitate. NMR analysis confirmed the identity of the product.
後処理
- temperaturecooling in an ice bath
- customremoved from the
- temperatureheat
- stirringstirred for an additional 10 minutes
- dissolutionThe reaction mixture was then dissolved in 50 ml of ether
- washwashed with water (1×30 ml), 5% NaOH (2×30 ml)
- dry with materialThe ether layer was dried over anhydrous sodium sulfate
- customthe solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-b34f90a0f2c94285b4d300023a88b43e
- 出典データセット
- uspto-grants-1996_06
- 特許番号
- US05525727
関連ノート
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