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

HRID 22244
ノート
印刷プレビュー

反応式

HRID 22244 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 178418406HCID 178418406、化合物触媒2 回HCID 6212Chloroform溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-4a4be547aa55439685a4cbd4c667d15f
出典データセット
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05428037

反応ノート

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