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3,4-Dimethylaniline → 3-[(3,4-Dimethylphenyl)amino)-4,6-dinitrophenol

HRID 1393587
노트
인쇄 미리보기

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HRID 1393587 반응식
[CH3:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[CH3:9])[NH2:5].[N+:10]([C:13]1[CH:18]=[C:17]([N+:19]([O-:21])=[O:20])[C:16]([OH:22])=[CH:15][C:14]=1F)([O-:12])=[O:11]>C(O)C>[CH3:1][C:2]1[CH:3]=[C:4]([NH:5][C:14]2[CH:15]=[C:16]([OH:22])[C:17]([N+:19]([O-:21])=[O:20])=[CH:18][C:13]=2[N+:10]([O-:12])=[O:11])[CH:6]=[CH:7][C:8]=1[CH3:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 72483,4-DimethylanilineHCID 150838855-Fluoro-2,4-dinitrophenol

생성물 1

HCID 219380413-[(3,4-Dimethylphenyl)amino)-4,6-dinitrophenol

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
40 °C

실험 절차

6.6 g of 3,4-dimethylaniline was added to a suspension that consists of 4 g of 4,6-dinitro-3-fluorophenol (J. Org. Chem. 1991, 5958) in 100 ml of ethanol, and it was stirred for 7 days at 40° C. After cooling, it was suctioned off, and the residue was recrystallized from ethanol.

후처리

  1. temperatureAfter cooling
  2. customthe residue was recrystallized from ethanol

출처 및 근거

ORD 기록
ord-b03ae106190c4cf68b5a7dd00b531ee0
출처 데이터셋
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07345075B2

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