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Aluminium lithium hydride → (4'-Fluoro-2-methoxy-biphenyl-4-yl)-methanol

HRID 2236467
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반응식

HRID 2236467 반응식
C[O:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)=[C:7]([O:18][CH3:19])[CH:6]=1)=O.[H-].[H-].[H-].[H-].[Li+].[Al+3]>CCOCC>[F:17][C:14]1[CH:13]=[CH:12][C:11]([C:8]2[CH:9]=[CH:10][C:5]([CH2:3][OH:2])=[CH:6][C:7]=2[O:18][CH3:19])=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 21226445Aluminium lithium hydrideHCID 592999004'-Fluoro-2-methoxy-biphenyl-4-carboxylic acid methyl ester

생성물 1

HCID 59300176(4'-Fluoro-2-methoxy-biphenyl-4-yl)-methanol

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

4′-Fluoro-2-methoxy-biphenyl-4-carboxylic acid methyl ester (220 mg, 0.85 mmol) is allowed to dissolve in ether and cooled. LiAlH4 (80 mg, 2.12 mmol) is then added and the suspension is then stirred overnight. After aqueous work up, the alcohol is isolated and used directly in the next step.

후처리

  1. temperaturecooled

출처 및 근거

ORD 기록
ord-70584e60d60644e79344b038ccb41efa
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07713994B2

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