Acetyl chloride → 4-(Acetoxymethyl)benzoic acid
反応式
C(N([CH2:6][CH3:7])CC)C.C(Cl)(=[O:10])C.[C:12]([O:15][CH2:16][CH3:17])(=[O:14])[CH3:13].[CH2:18]1[CH2:22][O:21][CH2:20][CH2:19]1>>[C:12]([O:15][CH2:16][C:17]1[CH:7]=[CH:6][C:19]([C:20]([OH:10])=[O:21])=[CH:18][CH:22]=1)(=[O:14])[CH3:13]参加物
5
反応条件
- 温度
- 0 °C
実験手順
Triethylamine (15.4 ml, 110.4 mmol) was added to a solution of aldehyde (2) (12.57 g, 92.4 mmol) in THF (50 ml) and cooled to 0° C. Acetyl chloride (7.91 g, 110.4 mmol) was then gradually added over 25 minutes, and the mixture was then left to stir for two hours at room temperature. After one hour, ethyl acetate (200 ml) was added and the solution washed with sodium carbonate (100 ml), HCl (17%, 50 ml) and water (100 ml) respectively. The organic layer was then dried over sodium sulfate and the solvent removed under reduced pressure to give an oil which crystallised when cooled. Re-crystallisation in methanol-hexane gave light yellow crystals.
後処理
- waitthe mixture was then left
- waitAfter one hour
- washthe solution washed with sodium carbonate (100 ml), HCl (17%, 50 ml) and water (100 ml) respectively
- dry with materialThe organic layer was then dried over sodium sulfate
- customthe solvent removed under reduced pressure
- customto give an oil which
- customcrystallised when
- temperaturecooled
- customRe-crystallisation in methanol-hexane gave light yellow crystals
出典と根拠
- ORDレコード
- ord-a7b7694e13ac4ecfa40ec9b5e46cffeb
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07365141B2
反応ノート
読み込み中…