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4'-Trifluoromethyl-biphenyl-3-carboxylic acid → 4'-(Trifluoromethyl)[1,1'-biphenyl]-3-methanol

HRID 1993021
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인쇄 미리보기

반응식

HRID 1993021 반응식
[F:1][C:2]([F:19])([F:18])[C:3]1[CH:8]=[CH:7][C:6]([C:9]2[CH:10]=[C:11]([CH:15]=[CH:16][CH:17]=2)[C:12](O)=[O:13])=[CH:5][CH:4]=1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[F:1][C:2]([F:18])([F:19])[C:3]1[CH:4]=[CH:5][C:6]([C:9]2[CH:10]=[C:11]([CH:15]=[CH:16][CH:17]=2)[CH2:12][OH:13])=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 27827184'-Trifluoromethyl-biphenyl-3-carboxylic acidHCID 21226445Aluminium lithium hydride

생성물 1

HCID 144680034'-(Trifluoromethyl)[1,1'-biphenyl]-3-methanol수율 94.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

The carboxylic acid 2.1 (13.3 g, 50 mmol) in anhydrous THF (100 mL) was added dropwise to LiAlH4 (2.9 g, 75 mmol) in anhydrous THF (150 mL) at 0° C. over 30 minutes. The resulting mixture was slowly warmed to room temperature and stirred for 4 hours. The reaction was slowly quenched with water (2.9 mL) at 0° C., 15% NaOH aqueous solution (2.9 mL) and another portion of water (8.7 mL). The mixture was dried over Na2SO4 and concentrated to give a white solid (11.9 g). The crude product (2.2) was used in the next step without further purification.

후처리

  1. customThe reaction was slowly quenched with water (2.9 mL) at 0° C.
  2. dry with materialThe mixture was dried over Na2SO4
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-4c3d9aa9309b45339bea54c3b767ab5a
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07649110B2

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