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Benzene → N-(4-methoxyphenyl)-4-nitro-3-methylbenzene carboximidoyl chloride

HRID 1197868
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HRID 1197868 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10](=O)[C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[C:13]([CH3:20])[CH:12]=2)=[CH:5][CH:4]=1.C1C=CC=CC=1.S(Cl)([Cl:30])=O>>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N:9]=[C:10]([Cl:30])[C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[C:13]([CH3:20])[CH:12]=2)=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 241BenzeneHCID 24386Thionyl ChlorideHCID 790964N-(4-methoxyphenyl)-3-methyl-4-nitrobenzamide

생성물 1

HCID 13633435N-(4-methoxyphenyl)-4-nitro-3-methylbenzene carboximidoyl chloride

실험 절차

14 g of N-(4-methoxyphenyl)-4-nitro-3-methyl benzamide in suspension in 70 ml of thionyl chloride were heated for 20 hours at reflux. The solvent was eliminated by entrainment with benzene, and after drying under reduced pressure at ambient temperature, 15 g of N-(4-methoxyphenyl)-4-nitro-3-methylbenzene carboximidoyl chloride melting towards 80° C. were obtained.

후처리

  1. temperatureat reflux
  • customafter drying under reduced pressure at ambient temperature
  • 출처 및 근거

    ORD 기록
    ord-d6a32888520145e7b0f7ea42659d374a
    출처 데이터셋
    uspto-grants-1994_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05278180

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