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1,5-Dimethyl-4-hydroxymethyl-2-(4-trifluoromethylphenyl)imidazole → 1,5-Dimethyl-4-formyl-2-(4-trifluoromethylphenyl)imidazole

HRID 1077826
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HRID 1077826 반응식
[CH3:1][N:2]1[C:6]([CH3:7])=[C:5]([CH2:8][OH:9])[N:4]=[C:3]1[C:10]1[CH:15]=[CH:14][C:13]([C:16]([F:19])([F:18])[F:17])=[CH:12][CH:11]=1>C(Cl)(Cl)Cl.[O-2].[O-2].[Mn+4]>[CH3:1][N:2]1[C:6]([CH3:7])=[C:5]([CH:8]=[O:9])[N:4]=[C:3]1[C:10]1[CH:15]=[CH:14][C:13]([C:16]([F:18])([F:19])[F:17])=[CH:12][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 194302591,5-Dimethyl-4-hydroxymethyl-2-(4-trifluoromethylphenyl)imidazole

생성물 1

HCID 152882331,5-Dimethyl-4-formyl-2-(4-trifluoromethylphenyl)imidazole수율 100.8%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매2회HCID 6212Chloroform용매

실험 절차

A mixture of 1,5-dimethyl-4-hydroxymethyl-2-(4-trifluoromethylphenyl)imidazole (0.5 g) and manganese dioxide (2 g) in 20 ml of chloroform was refluxed for 24 hours. A further 2 g of manganese dioxide was added, and the mixture refluxed for a further 3 hours. The mixture was cooled, the solid material filtered off, and washed with methylene chloride. The solvent was removed from the filtrate under reduced pressure, to yield 0.5 g of 1,5-dimethyl-4-formyl-2-(4-trifluoromethylphenyl)imidazole, m.p. 144° C.

후처리

  1. temperaturewas refluxed for 24 hours
  2. temperaturethe mixture refluxed for a further 3 hours
  3. temperatureThe mixture was cooled
  4. filtrationthe solid material filtered off
  5. washwashed with methylene chloride
  6. customThe solvent was removed from the filtrate under reduced pressure

출처 및 근거

ORD 기록
ord-f82b6696795142aeaf77fe51695f9524
출처 데이터셋
uspto-grants-1996_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05545645

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