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HCID 135696401, 화합물 → HCID 135665331, 화합물

HRID 2260244
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HRID 2260244 반응식
[N:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[NH:3][C:2]=1[C:10]1[CH:15]=[C:14]([N+:16]([O-:18])=[O:17])[C:13]([OH:19])=[C:12]([O:20]C)[CH:11]=1>C(O)(=O)C.Br>[N:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[NH:3][C:2]=1[C:10]1[CH:11]=[C:12]([OH:20])[C:13]([OH:19])=[C:14]([N+:16]([O-:18])=[O:17])[CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 135696401HCID 135696401, 화합물

생성물 1

HCID 135665331HCID 135665331, 화합물

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 260Hydrogen Bromide용매

실험 절차

A suspension of 860.1 mg of 4-(2-benzimidazolyl)-2-methoxy-6-nitrophenol in 10 ml of glacial acetic acid and 10 ml of 48 percent hydrobromic acid is heated to boiling under reflux for 72 hours. The mixture is then evaporated and the residue is treated four times with 50 ml of toluene each time, which is again distilled each time. There is obtained 5-(2-benzimidazolyl)-3-nitropyrocatechol of m.p.>300° (from acetone/water).

후처리

  1. temperatureis heated
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • temperatureunder reflux for 72 hours
  • customThe mixture is then evaporated
  • additionthe residue is treated four times with 50 ml of toluene each time, which
  • distillationis again distilled each time
  • 출처 및 근거

    ORD 기록
    ord-f3dddf6e071c4b1ea30625a683a14f39
    출처 데이터셋
    uspto-grants-1995_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05476875

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