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Indoline → 1-(2-Nitrophenyl)indoline

HRID 2052687
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인쇄 미리보기

반응식

HRID 2052687 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.F[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[N+:17]([O-:19])=[O:18]>>[N+:17]([C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=1[N:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1)([O-:19])=[O:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 10328IndolineHCID 738951-Fluoro-2-nitrobenzene

생성물 1

HCID 74105181-(2-Nitrophenyl)indoline

반응 조건

온도
120 °C

실험 절차

11.0 g (0.10 mole) of indoline and 28.2 g of 1-fluoro-2-nitrobenzene are combined and the resultant solution is stirred and heated to 120° C. and kept at that temperature 18 hours. The reaction mixture is then cooled to room temperature and partitioned between chloroform and water. The chloroform layer is separated, washed with water, dried and concentrated in vacuum. The residue is dissolved in isopropylether from which 1-(2-nitrophenyl)indoline, m.p. 62°-64° C., precipitates on standing.

후처리

  1. customkept at that temperature 18 hours
  2. temperatureThe reaction mixture is then cooled to room temperature
custom
partitioned between chloroform and water
  • customThe chloroform layer is separated
  • washwashed with water
  • customdried
  • concentrationconcentrated in vacuum
  • dissolutionThe residue is dissolved in isopropylether from which 1-(2-nitrophenyl)indoline, m.p. 62°-64° C.
  • customprecipitates
  • 출처 및 근거

    ORD 기록
    ord-7f61eed643c049daa497e4313c3a42d2
    출처 데이터셋
    uspto-grants-1980_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04186199

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