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O-Toluidine → HCID 53269523, 화합물

HRID 2054623
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HRID 2054623 반응식
[NH2:1][C:2]1[C:3]([CH3:8])=[CH:4][CH:5]=[CH:6][CH:7]=1.[Cl:9][C:10]1[CH:15]=[CH:14][C:13]([N+:16]([O-:18])=[O:17])=[C:12]([N+]([O-])=O)[CH:11]=1>C(O)C>[Cl:9][C:10]1[CH:11]=[CH:12][C:13]([N+:16]([O-:18])=[O:17])=[C:14]([NH:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=2[CH3:8])[CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7242O-ToluidineHCID 330974-Chloro-1,2-dinitrobenzene

생성물 1

HCID 53269523HCID 53269523, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

81 ml of o-toluidine was added to absolution of 10 g of 1-chloro-3,4-dinitrobenzene in 50 ml of ethanol, and it was refluxed for 72 hours. It was concentrated by evaporation in a vacuum, the residue was taken up in ethyl acetate and 2N aqueous hydrochloric acid. The organic phase was extracted three more times with 2N aqueous hydrochloric acid, dried on sodium sulfate and concentrated by evaporation in a vacuum. The residue was purified by chromatography on silica gel.

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이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
was refluxed for 72 hours
  • concentrationIt was concentrated by evaporation in a vacuum
  • extractionThe organic phase was extracted three more times with 2N aqueous hydrochloric acid
  • customdried on sodium sulfate
  • concentrationconcentrated by evaporation in a vacuum
  • customThe residue was purified by chromatography on silica gel
  • 출처 및 근거

    ORD 기록
    ord-2c01918b973547cd929ab2a8067028c0
    출처 데이터셋
    uspto-grants-2008_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07329679B2

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