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Pyrrole → 3-Fluoro-1-nitro-4-(1H-pyrrol-1-yl)benzene

HRID 56128
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인쇄 미리보기

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HRID 56128 반응식
F[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][C:3]=1[F:11].C([O-])([O-])=O.[K+].[K+].[NH:18]1[CH:22]=[CH:21][CH:20]=[CH:19]1>CS(C)=O.O>[F:11][C:3]1[CH:4]=[C:5]([N+:8]([O-:10])=[O:9])[CH:6]=[CH:7][C:2]=1[N:18]1[CH:22]=[CH:21][CH:20]=[CH:19]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8027PyrroleHCID 11430Potassium CarbonateHCID 1230531,2-Difluoro-4-nitrobenzene

생성물 1

HCID 107034583-Fluoro-1-nitro-4-(1H-pyrrol-1-yl)benzene수율 97%

시약·촉매·용매 2

HCID 679Dimethyl Sulfoxide용매HCID 962Water용매

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온도
90 °C

실험 절차

To a solution of 1,2-difluoro-4-nitrobenzene (1.59 g, 10 mmol) in DMSO (15 mL) were added K2CO3 (3.04 g, 22 mmol) and pyrrole (0.74 g, 11 mmol) with stirring. The reaction mixture was heated at 90° C. for 18 h, and cooled to rt. The mixture was diluted with water (50 mL), filtered and the filter cake was dried to give the title compound as a yellow solid (2.00 g, 97%).

후처리

  1. temperaturecooled to rt
  2. filtrationfiltered
  3. customthe filter cake was dried

출처 및 근거

ORD 기록
ord-d97e250c56b54b6ea7fde21ea169c008
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434695B2

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