Benzyl Bromide → 2-(6-Benzyloxy-2,5,7,8-tetramethylchroman-2-yl)ethanol
反応式
[OH:1][C:2]1[C:3]([CH3:18])=[C:4]2[C:9](=[C:10]([CH3:13])[C:11]=1[CH3:12])[O:8][C:7]([CH2:15][CH2:16][OH:17])([CH3:14])[CH2:6][CH2:5]2.[CH2:19](Br)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1>>[CH2:19]([O:1][C:2]1[C:3]([CH3:18])=[C:4]2[C:9](=[C:10]([CH3:13])[C:11]=1[CH3:12])[O:8][C:7]([CH2:15][CH2:16][OH:17])([CH3:14])[CH2:6][CH2:5]2)[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1参加物
3
実験手順
Following the procedure described in Preparation 1, 2-(6-hydroxy-2,5,7,8-tetramethylchroman-2-yl)ethanol was reacted with benzyl bromide and treated and purified to give the title compound.
後処理
- additiontreated
- custompurified
出典と根拠
- ORDレコード
- ord-ae44596f4d4741ccb6865b96fca99299
- 出典データセット
- uspto-grants-1986_02
- 特許番号
- US04572912
反応ノート
読み込み中…