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Hydrochloric Acid → 5-chloro-2-(4-nitrophenyl)-1H-Imidazole-4-carboxaldehyde

HRID 350586
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HRID 350586 반응식
[ClH:1].[N+:2]([C:5]1[CH:18]=[CH:17][C:8]([CH:9]=[N:10][C:11](=[C:14](Cl)Cl)[C:12]#[N:13])=[CH:7][CH:6]=1)([O-:4])=[O:3].[O:19]1CCOCC1>>[Cl:1][C:12]1[N:13]=[C:9]([C:8]2[CH:17]=[CH:18][C:5]([N+:2]([O-:4])=[O:3])=[CH:6][CH:7]=2)[NH:10][C:11]=1[CH:14]=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 312751,4-DioxaneHCID 122907202-(4-Nitrobenzylidene)amino-3,3-dichloropropenonitrile

생성물 1

HCID 1785200115-chloro-2-(4-nitrophenyl)-1H-Imidazole-4-carboxaldehyde

실험 절차

HCl gas was bubbled through a solution of 2-(4-nitrobenzylidene)amino-3,3-dichloro-propenonitrile (40.0 g, 0.148 mole) in dioxane (500 ml) at room temperature. The mixture was stirred for 23 hours at 50 ΕC. HCl gas was bubbled through followed by stirring for 24 hours at 50 ΕC. The mixture was stirred for 8 more days at 50 ΕC with addition of HCl-gas every 24 hours, followed by stirring at 50 ΕC for 4 more days. More HCl-gas was added and stirred for 3 more days at 50 ΕC. The solution was cooled to 0 ΕC and filtered. The residue was mixed with ethanol (96%, 200 ml) and the title compound, Compound 6, was isolated by filration. Yield: 23.1 g (62%). NMR confirmed the structure of the title compound.

후처리

  1. customHCl gas was bubbled
  2. stirringby stirring for 24 hours at 50 ΕC
  3. stirringThe mixture was stirred for 8 more days at 50 ΕC with addition of HCl-gas every 24 hours
  4. stirringby stirring at 50 ΕC for 4 more days
  5. additionMore HCl-gas was added
  6. stirringstirred for 3 more days at 50 ΕC
  7. temperatureThe solution was cooled to 0 ΕC
  8. filtrationfiltered
  9. additionThe residue was mixed with ethanol (96%, 200 ml)

출처 및 근거

ORD 기록
ord-d47d920d66a24f8396e43f6990bae139
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07182934B2

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