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P-Anisidine → HCID 178492142, 화합물

HRID 1985775
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반응식

HRID 1985775 반응식
[OH:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][N:3]=1.[CH3:9][O:10][C:11]1[CH:17]=[CH:16][C:14]([NH2:15])=[CH:13][CH:12]=1>O.CC(C)=O>[CH3:9][O:10][C:11]1[CH:17]=[CH:16][C:14]([NH:15][C:5]2[C:4]([NH:15][C:14]3[CH:16]=[CH:17][C:11]([O:10][CH3:9])=[CH:12][CH:13]=3)=[N:3][C:2](=[O:1])[C:7](=[O:8])[CH:6]=2)=[CH:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7732P-AnisidineHCID 178516237HCID 178516237, 화합물

생성물 1

HCID 178492142HCID 178492142, 화합물수율 32%

시약·촉매·용매 1

HCID 18366337Propan-2-one--water (1/1)용매

실험 절차

2,3-dihydroxypyridine (0.0027 mol), p-methoxyaniline (0.0054 mol); and NaIO3 (0.0009 mol) were dissolved in 160 ml of water/acetone (80:1, v/v) solvent. The reaction mixture was stirred for 2 hours, and maintained still overnight. It was then filtered, and recrystallized with chloroform. The final product was 5,6-di(p-methoxyphenylamino)-2,3-pyridindione in a red powder. The yield was 32%-50%.

후처리

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  • temperaturemaintained still overnight
  • filtrationIt was then filtered
  • customrecrystallized with chloroform
  • 출처 및 근거

    ORD 기록
    ord-5bfc5170b7b249ba9d521dab933c6976
    출처 데이터셋
    uspto-grants-2009_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07547713B2

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