Aluminium lithium hydride → 2-(2,3-dihydro-1H-indol-1-yl)ethan-1-ol
反応式
[N:1]1([CH2:10][C:11](OC)=[O:12])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[N:1]1([CH2:10][CH2:11][OH:12])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1参加物
4
実験手順
A procedure similar to that described in Preparation was repeated, except that 780 mg of methyl indolin-1-ylacetate (prepared as described in preparation 8), mg of lithium aluminum hydride and 12 ml of anhydrous tetrahydrofuran were used, to give 580 mg of the title compound having Rf=0.31 (on silica gel thin layer chromatography using a 2:1 by volume mixture of hexane and ethyl acetate as the developing solvent).
後処理
- customA procedure similar to that described in Preparation
出典と根拠
- ORDレコード
- ord-29cb5c1c9912439e8882a3b313eb7604
- 出典データセット
- uspto-grants-1998_04
- 特許番号
- US05739345
反応ノート
読み込み中…