Sodium borohydride → [3-(4-Bromo-2-hydroxymethyl-phenoxy)-phenyl]-acetic acid ethyl ester
反応式
[CH2:1]([O:3][C:4](=[O:22])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([O:12][C:13]2[CH:18]=[CH:17][C:16]([Br:19])=[CH:15][C:14]=2[CH:20]=[O:21])[CH:7]=1)[CH3:2].[BH4-].[Na+]>CO>[CH2:1]([O:3][C:4](=[O:22])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([O:12][C:13]2[CH:18]=[CH:17][C:16]([Br:19])=[CH:15][C:14]=2[CH2:20][OH:21])[CH:7]=1)[CH3:2]参加物
4
実験手順
To [3-(4-bromo-2-formyl-phenoxy)-phenyl]-acetic acid ethyl ester (0.70 g, 1.9 mmol) in MeOH (20 mL) was added sodium borohydride (0.07 g, 1.9 mmol), and the reaction was stirred for 5 minutes at room temperature. Once no starting material was seen by analytical tlc, the mixture was worked-up to give the desired product (0.7 g).
出典と根拠
- ORDレコード
- ord-695d6a9b6af849759a98920607090aec
- 出典データセット
- uspto-grants-2012_08
- 特許番号
- US08242145B2
反応ノート
読み込み中…