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O-Phenylenediamine → 2-(1,3-benzodioxol-5-yl)-1H-benzimidazole

HRID 366852
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반응식

HRID 366852 반응식
[CH:1]1[C:6]([CH:7]=O)=[CH:5][C:4]2[O:9][CH2:10][O:11][C:3]=2[CH:2]=1.[C:12]1([NH2:19])[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[NH2:18]>[N+](C1C=CC=CC=1)([O-])=O>[O:11]1[C:3]2[CH:2]=[CH:1][C:6]([C:7]3[NH:19][C:12]4[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=4[N:18]=3)=[CH:5][C:4]=2[O:9][CH2:10]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7243O-PhenylenediamineHCID 8438Piperonal

생성물 1

HCID 2429622-(1,3-benzodioxol-5-yl)-1H-benzimidazole수율 49%

시약·촉매·용매 1

HCID 7416Nitrobenzene용매

실험 절차

A solution of 50 g (0.34 mol) of piperonal and 37 g (0.34 mol) of phenylenediamine in 0.3 L of nitrobenzene was stirred under reflux for 12 hours. The resulting mixture was concentrated in vacuo. The solid residue was collected via filtration, and rinsed with ether to give 39.6 g (49%) of desired material as an off-white solid: 1H NMR (CDCl3) δ 5.96 (s, 2H), 6.79 (d, J=8.5 Hz, 1H), 7.17-7.30 (m, 2H), 7.50-7.65 (m, 4H), 8.80-9.40 (br s, 1H).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. temperatureunder reflux for 12 hours
  2. concentrationThe resulting mixture was concentrated in vacuo
  3. filtrationThe solid residue was collected via filtration
  4. washrinsed with ether

출처 및 근거

ORD 기록
ord-1083927ef4f84be38a5e87d42ce324ea
출처 데이터셋
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06130333

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