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O-Phenylenediamine → HCID 135696401, 화합물

HRID 725341
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HRID 725341 반응식
[N+:1]([C:4]1[C:5]([OH:14])=[C:6]([O:12][CH3:13])[CH:7]=[C:8]([CH:11]=1)[CH:9]=O)([O-:3])=[O:2].[C:15]1([NH2:22])[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[NH2:21].[N+](C1C=CC=CC=1)([O-])=O>CO>[N:21]1[C:16]2[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=2[NH:22][C:9]=1[C:8]1[CH:11]=[C:4]([N+:1]([O-:3])=[O:2])[C:5]([OH:14])=[C:6]([O:12][CH3:13])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7243O-PhenylenediamineHCID 7416NitrobenzeneHCID 811345-Nitrovanillin

생성물 1

HCID 135696401HCID 135696401, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

aa) A solution of 4.93 g of 5-nitrovanillin and 2.7 g of 1,2-phenylenediamine, in 45 ml of methanol and 15 ml of nitrobenzene is heated to boiling under reflux. After 15 minutes crystals begin to separate from the red solution. After 18 hours the reaction mixture is cooled to room temperature and diluted with 60 ml of methanol. The crystals are filtered under suction and washed with methanol. There is obtained 4-(2-benzimidazolyl)-2-methoxy-6-nitrophenol of m.p. 198°-200° (from N,N-dimethylformamide/methanol).

후처리

  1. temperatureunder reflux
  2. customto separate from the red solution
  3. additiondiluted with 60 ml of methanol
  4. filtrationThe crystals are filtered under suction
  5. washwashed with methanol

출처 및 근거

ORD 기록
ord-2c8e17cd62424670be8de54ece1afab3
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05705703

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