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6,7-Dichloro-5-hydroxy-2,2-dimethyl-indan-1-one → 2,2-Dimethyl-6,7-dichloro-1,5-indanediol

HRID 597003
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반응식

HRID 597003 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 123955876,7-Dichloro-5-hydroxy-2,2-dimethyl-indan-1-oneHCID 21584525Sodium bis(2-methoxyethoxy)aluminiumhydride

생성물 1

HCID 214494882,2-Dimethyl-6,7-dichloro-1,5-indanediol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

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.

후처리

  1. custom2,2-Dimethyl-6,7-dichloro-1,5-indanediol is prepared

출처 및 근거

ORD 기록
ord-c5dc353dcc3745b08c4de033e7e5275c
출처 데이터셋
uspto-grants-1977_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04012524

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