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1,1'-Biphenyl, mixt. with 1,1'-oxybis(benzene) → HCID 178469560, 화합물

HRID 48289
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인쇄 미리보기

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HRID 48289 반응식
[F:1][C:2]([F:19])([F:18])[C:3]1[CH:4]=[C:5]([CH:15]=[CH:16][CH:17]=1)[NH:6][CH:7]=[C:8]([C:12]([O-:14])=O)[C:9]([O-:11])=[O:10].[CH:20]1C=CC(C2C=CC=CC=2)=C[CH:21]=1.C1C=CC(OC2C=CC=CC=2)=CC=1>>[OH:14][C:12]1[C:15]2[C:5](=[CH:4][C:3]([C:2]([F:1])([F:19])[F:18])=[CH:17][CH:16]=2)[N:6]=[CH:7][C:8]=1[C:9]([O:11][CH2:20][CH3:21])=[O:10]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 246701,1'-Biphenyl, mixt. with 1,1'-oxybis(benzene)HCID 226483082-{[3-(Trifluoromethyl)anilino]methylene}malonate

생성물 1

HCID 178469560HCID 178469560, 화합물

반응 조건

온도
240 °C

실험 절차

Under a nitrogen atmosphere, a mixture of 2-{[3-(trifluoromethyl)anilino]methylene}malonate (80 g, 0.24 mol) and Dowtherm A was heated to 240° C. and then stirred for 3 hours. The reaction mixture was allowed to cool to ambient temperature and then stirred for 16 hours. The solids were isolated by filtration then washed with hexane to provide 47.5 g of ethyl 4-hydroxy-7-(trifluoromethyl)-3-quinolinecarboxylate as an off-white solid.

후처리

  1. temperature
to cool to ambient temperature
  • stirringstirred for 16 hours
  • customThe solids were isolated by filtration
  • washthen washed with hexane
  • 출처 및 근거

    ORD 기록
    ord-f6a378c9d38b4ea78fc777c5acce1586
    출처 데이터셋
    uspto-grants-2004_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06703402B2

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