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3,4-Dinitrophenol → 4-(3,4-Dinitrophenoxy)-6,7-dimethoxyquinoline

HRID 491669
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인쇄 미리보기

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HRID 491669 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][CH:7]=[C:6]2Cl.[N+:16]([C:19]1[CH:20]=[C:21]([OH:28])[CH:22]=[CH:23][C:24]=1[N+:25]([O-:27])=[O:26])([O-:18])=[O:17]>CO>[N+:16]([C:19]1[CH:20]=[C:21]([CH:22]=[CH:23][C:24]=1[N+:25]([O-:27])=[O:26])[O:28][C:6]1[C:5]2[C:10](=[CH:11][C:12]([O:13][CH3:14])=[C:3]([O:2][CH3:1])[CH:4]=2)[N:9]=[CH:8][CH:7]=1)([O-:18])=[O:17]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 113483,4-DinitrophenolHCID 4596104-Chloro-6,7-dimethoxyquinoline

생성물 1

HCID 177563934-(3,4-Dinitrophenoxy)-6,7-dimethoxyquinoline

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
150 °C

실험 절차

A mixture of 6,7-dimethoxy-4-chloroquinoline (0.35 g, 1.6 mmol) and 3,4-dinitrophenol (0.85 g, 4.6 mmol) was heated to 150° C. for 4 h. The mixture was cooled at RT and MeOH added. The reaction was stirred for 3 h. The precipitate filtered out and was washed with MeOH to afford 4-(3,4-dinitrophenoxy)-6,7-dimethoxyquinoline.

후처리

  1. temperatureThe mixture was cooled at RT
  2. filtrationThe precipitate filtered out
  3. washwas washed with MeOH

출처 및 근거

ORD 기록
ord-97f2b4e341514bf8995ed2ea4747d2ad
출처 데이터셋
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07531553B2

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