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Acetone → 4'-Trifluoromethoxy-biphenyl-4-carboxylic acid

HRID 1470608
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인쇄 미리보기

반응식

HRID 1470608 반응식
[F:1][C:2]([F:19])([F:18])[O:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[CH:15]=[CH:14][C:13]([CH:16]=[O:17])=[CH:12][CH:11]=2)=[CH:6][CH:5]=1.CC(C)=[O:22]>>[F:1][C:2]([F:18])([F:19])[O:3][C:4]1[CH:5]=[CH:6][C:7]([C:10]2[CH:15]=[CH:14][C:13]([C:16]([OH:22])=[O:17])=[CH:12][CH:11]=2)=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 180AcetoneHCID 27607204'-Trifluoromethoxy-biphenyl-4-carbaldehyde

생성물 1

HCID 27607234'-Trifluoromethoxy-biphenyl-4-carboxylic acid수율 77%

실험 절차

To a cold solution of 4′-trifluoromethoxy-biphenyl-4-carbaldehyde (0.9 g, 3.38 mmol) in acetone (10 mL) the Jone's reagent was added slowly at 0° C. drop wise until reaction completes. Acetone was removed completely and the residue was diluted with water, extracted with ethyl acetate and the combined organic layers were washed with water and brine, dried over sodium sulphate and concentrated to obtain the title compound (0.7 g, 77%).

후처리

  1. customwise until reaction
  2. customAcetone was removed completely
  3. additionthe residue was diluted with water
  4. extractionextracted with ethyl acetate
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
wash
the combined organic layers were washed with water and brine
  • dry with materialdried over sodium sulphate
  • concentrationconcentrated
  • 출처 및 근거

    ORD 기록
    ord-0e1e5ab2712342a9879e0e4ed676f391
    출처 데이터셋
    uspto-grants-2015_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09006454B2

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