Ethyl bromoacetate → 2-[3-Hydroxy-5-[hydroxymethyl]phenyloxy]acetic acid, ethyl ester
反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([OH:10])[CH:9]=1)[CH2:5][OH:6].Br[CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14]>>[OH:1][C:2]1[CH:9]=[C:8]([O:10][CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH:7]=[C:4]([CH2:5][OH:6])[CH:3]=1参加物
3
実験手順
the subtitle compound was prepared from 3,5-dihydroxybenzyl alcohol (5 g) and ethyl bromoacetate (5.96 g) by the method of example 21 step (ii). Purified by chromatography eluting with 30% ethyl acetate in isohexane. Yield 1.6 g.
後処理
- customPurified by chromatography
- washeluting with 30% ethyl acetate in isohexane
出典と根拠
- ORDレコード
- ord-73387faa66d54a03a2d15275ebeac7c2
- 出典データセット
- uspto-grants-2001_03
- 特許番号
- US06200981B1
反応ノート
読み込み中…