Methyl bromoacetate → 3-Bromo-2-methoxyphenoxyacetic acid methyl ester
反応式
[Br:1][C:2]1[C:3]([O:9][CH3:10])=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.Br[CH2:12][C:13]([O:15][CH3:16])=[O:14]>>[CH3:16][O:15][C:13](=[O:14])[CH2:12][O:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([Br:1])[C:3]=1[O:9][CH3:10]参加物
3
実験手順
The compound of Formula XVIII wherein s is zero can also be prepared by treating 3-bromo-2-methoxyphenol with methyl bromoacetate to give 3-bromo-2-methoxyphenoxyacetic acid methyl ester which is reduced to the alcohol using, e.g., diisobutylaluminum hydride with subsequent protection of the alcohol with an R12 protecting group as generally described hereinbefore.
後処理
- customcan also be prepared
出典と根拠
- ORDレコード
- ord-992ba6eabc2d43408cdc5486d3186ed8
- 出典データセット
- uspto-grants-1983_08
- 特許番号
- US04401824
反応ノート
読み込み中…