6,7-Dichloro-5-hydroxy-2,2-dimethyl-indan-1-one → 2,2-Dimethyl-6,7-dichloro-1,5-indanediol
反応式
[CH3:1][C:2]1([CH3:15])[CH2:10][C:9]2[C:4](=[C:5]([Cl:13])[C:6]([Cl:12])=[C:7]([OH:11])[CH:8]=2)[C:3]1=[O:14].[H-].COCCO[Al+]OCCOC.[Na+].[H-]>O1CCCC1>[CH3:1][C:2]1([CH3:15])[CH2:10][C:9]2[C:4](=[C:5]([Cl:13])[C:6]([Cl:12])=[C:7]([OH:11])[CH:8]=2)[CH:3]1[OH:14]参加物
4
実験手順
2,2-Dimethyl-6,7-dichloro-1,5-indanediol is prepared following substantially the same procedure described in Example 4, Step E, using the following substances: 2,2-dimethyl-5-hydroxy-6,7-dichloro-1-indanone (6.1 g., 0.025 mole); sodium bis-(2-methoxyethoxy)-aluminum hydride (70% in benzene) 8 ml.; tetrahydrofuran (75 ml.). The above procedure gives 2,2-dimethyl-6,7-dichloro-1,5-indanediol.
後処理
- custom2,2-Dimethyl-6,7-dichloro-1,5-indanediol is prepared
出典と根拠
- ORDレコード
- ord-c5dc353dcc3745b08c4de033e7e5275c
- 出典データセット
- uspto-grants-1977_03
- 特許番号
- US04012524
反応ノート
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