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O-Phenylenediamine → 2-((4-Phenoxyphenyl)sulfonylamino)aniline

HRID 1419435
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인쇄 미리보기

반응식

HRID 1419435 반응식
[O:1]([C:8]1[CH:13]=[CH:12][C:11]([S:14](Cl)(=[O:16])=[O:15])=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:18]1([NH2:25])[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[NH2:24]>CCCCCC>[O:1]([C:8]1[CH:13]=[CH:12][C:11]([S:14]([NH:24][C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=2[NH2:25])(=[O:16])=[O:15])=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7243O-PhenylenediamineHCID 27947564-Phenoxybenzene-1-sulfonyl chloride

생성물 1

HCID 211847012-((4-Phenoxyphenyl)sulfonylamino)aniline

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

The title compound was prepared according to General Method C using 4-phenoxyphenylsulfonyl chloride (969 mg, 3.6 mmol) and o-phenylenediamine (300 mg, 2.77 mmol). The reaction mixture was partitioned between water (200 ml) and toluene:methylene chloride (1:3). The organic phase collected and the methylene chloride evaporated leaving the toluene. Hexane added and the product precipatated from solution. (317 mg, 34%) EI-MS m/z 341 (M+H)+

후처리

  1. customThe reaction mixture was partitioned between water (200 ml) and toluene:methylene chloride (1:3)
  2. customThe organic phase collected
  3. customthe methylene chloride evaporated
  4. customleaving the toluene

출처 및 근거

ORD 기록
ord-df0b1501518a4c40898900ee768a77dc
출처 데이터셋
uspto-grants-1999_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05886044

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