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O-Phenylenediamine → 2,3-Bis(4-aminophenyl)-quinoxaline

HRID 1796959
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인쇄 미리보기

반응식

HRID 1796959 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:10]([C:12]2[CH:17]=[CH:16][C:15]([NH2:18])=[CH:14][CH:13]=2)=O)=O)=[CH:4][CH:3]=1.[C:19]1([NH2:26])[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[NH2:25]>C(O)(=O)C>[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:10]([C:12]3[CH:17]=[CH:16][C:15]([NH2:18])=[CH:14][CH:13]=3)=[N:26][C:19]3[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=3)[N:25]=2)=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7243O-PhenylenediamineHCID 2751371,2-Bis(4-aminophenyl)-1,2-ethanedione

생성물 1

HCID 4591452,3-Bis(4-aminophenyl)-quinoxaline

시약·촉매·용매 1

HCID 176Acetic Acid용매

반응 조건

온도
50 °C

실험 절차

A mixture of 1.0 g (4.17 mmole) of 4,4′-diaminobenzil and 0.45 g of o-phenylenediamine in 250 ml glacial acetic acid was heated at 50° C. for 15 mins., then stirred for 16 hours at room temperature. The mixture was then heated to 80° C. and allowed to cool slowly. The solvent was removed under vacuum and the residue was redissolved in ethanol and that was removed under vacuum.

후처리

  1. temperatureThe mixture was then heated to 80° C.
  2. temperatureto cool slowly
  3. customThe solvent was removed under vacuum
  4. dissolutionthe residue was redissolved in ethanol
  5. customthat was removed under vacuum

출처 및 근거

ORD 기록
ord-ae4cc4d8f82c4b0a8705dcec0abc13ab
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07034026B2

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