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Nitrobenzene → 4'-Fluoro-2'-methoxy-4-nitrobiphenyl

HRID 442265
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HRID 442265 반응식
[F:1][C:2]1[CH:8]=[CH:7][C:5](N)=[C:4]([O:9][CH3:10])[CH:3]=1.[N+:11]([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([O-:13])=[O:12].N(OCCC(C)C)=O>>[F:1][C:2]1[CH:8]=[CH:7][C:5]([C:17]2[CH:18]=[CH:19][C:14]([N+:11]([O-:13])=[O:12])=[CH:15][CH:16]=2)=[C:4]([O:9][CH3:10])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 7416NitrobenzeneHCID 8053Isoamyl NitriteHCID 135322284-Fluoro-2-methoxyaniline

생성물 1

HCID 214164654'-Fluoro-2'-methoxy-4-nitrobiphenyl

실험 절차

A mixture of 7.7 grams of 4-fluoro-2-methoxyaniline, 200 ml. of nitrobenzene, and 9.0 grams of isoamyl nitrite, is warmed on the steam bath until a vigorous reaction with evolution of gas sets in. This evolution is allowed to proceed without heating until it has subsided, and the mixture is then heated on the steam bath for an additional 3 hours. The excess of nitrobenzene is removed in vacuo. The residue is purified for the desired isomer by elution from a silica gel column using petroleum-benzin to yield 4'-fluoro-2'-methoxy-4-nitrobiphenyl.

후처리

  1. temperature
without heating until it
  • temperaturethe mixture is then heated on the steam bath for an additional 3 hours
  • customThe excess of nitrobenzene is removed in vacuo
  • customThe residue is purified for the desired isomer
  • washby elution from a silica gel column
  • 출처 및 근거

    ORD 기록
    ord-538a0af40cf44d548c344234dbeb97e5
    출처 데이터셋
    uspto-grants-1977_08
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04044049

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