Hydrochloric Acid → 6-Acetoxy-2-hydroxy-2,5,7,8-tetramethylchroman
反応式
[C:1]([O:4][C:5]1[C:6]([CH3:20])=[C:7]2[C:12](=[C:13]([CH3:16])[C:14]=1[CH3:15])[O:11][C:10]([O:18]C)([CH3:17])[CH2:9][CH2:8]2)(=[O:3])[CH3:2].Cl>CC(C)=O>[C:1]([O:4][C:5]1[C:6]([CH3:20])=[C:7]2[C:12](=[C:13]([CH3:16])[C:14]=1[CH3:15])[O:11][C:10]([OH:18])([CH3:17])[CH2:9][CH2:8]2)(=[O:3])[CH3:2]参加物
実験手順
To a solution of (±)-6-acetoxy-2-methoxy-2,5,7,8-tetramethylchroman in 2500 ml. of acetone was added 2000 ml. of H 2 O followed by 16.6 ml. of concentrated aqueous HCl. Solvent was distilled from the stirred mixture until the head temperature reached 90° centigrade. The suspension was cooled in an H 2 O bath to 50° centigrade. At 70° centigrade, 2000 ml. of acetone was added, giving a clear solution. The solution was seeded occasionally until crystallization began. After 3.5 hours, 1500 ml. of H 2 O was added and the suspension was cooled in an ice bath. The solid was removed by filtration, washed with H 2 O and dried at 50° centigrade/0.1mmHg. to give (±)-6-acetoxy-2-hydroxy-2,5,7,8-tetramethylchroman as a granular yellow-tan solid, sintering from 114 degrees centigrade, m.p. 127°-132° centigrade.
後処理
- distillationSolvent was distilled from the stirred mixture until the head temperature
- customreached 90°
- temperatureThe suspension was cooled in an H 2 O bath to 50° centigrade
- customAt 70°
- additionof acetone was added
- customgiving a clear solution
- customThe solution was seeded occasionally until crystallization
- additionof H 2 O was added
- temperaturethe suspension was cooled in an ice bath
- customThe solid was removed by filtration
- washwashed with H 2 O
- customdried at 50° centigrade/0.1mmHg
出典と根拠
- ORDレコード
- ord-6c2522f3e18d4b66931378ceb4394978
- 出典データセット
- uspto-grants-1977_04
- 特許番号
- US04018799
反応ノート
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