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Formaldehyde → [2-(4-Methylphenyl)-1H-imidazole-4,5-diyl]dimethanol

HRID 2419119
ノート
印刷プレビュー

反応式

HRID 2419119 の反応式
[C:1]1([CH3:12])[CH:6]=[CH:5][C:4]([C:7]2[NH:8][CH:9]=[CH:10][N:11]=2)=[CH:3][CH:2]=1.C=O.[C:15](=[O:18])([O-])[O-].[K+].[K+].[CH3:21][O:22]CCO>O>[C:1]1([CH3:12])[CH:2]=[CH:3][C:4]([C:7]2[NH:11][C:10]([CH2:15][OH:18])=[C:9]([CH2:21][OH:22])[N:8]=2)=[CH:5][CH:6]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 712FormaldehydeHCID 80192-MethoxyethanolHCID 11430Potassium CarbonateHCID 5940452-(4-Methylphenyl)-1H-imidazole

生成物 1

HCID 22764401[2-(4-Methylphenyl)-1H-imidazole-4,5-diyl]dimethanol収率 21%

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
95 °C

実験手順

A mixture of 15.8 g (0.1 mole) of 2-p-tolyl imidazole, 9 g (0.3 mole) of paraformaldehyde, 2 g (0.015 mole) of potassium carbonate, and 50 ml of methyl cellosolve was heated at 95° C. for 30 minutes with stirring in the same way as in Example 1. 200 ml of water was added, and the reaction mixture was boiled for a while and cooled. The crystals were collected by filtration, boiled together with 20 ml of toluene, and cooled. The crystals were collected by filtration and recrystallized from methyl cellosolve to afford 2-p-tolyl-4,5-dihydroxymethyl imidazole as a final product in an amount of 4.5 g (yield 21%). The thin-layer chromatography (cellulose:n-BuOH:AcOH:W = 4:1:2) of the crystals gave only one spot at Rf = 0.73.

後処理

  1. temperaturecooled
  2. filtrationThe crystals were collected by filtration
  3. temperaturecooled
  4. filtrationThe crystals were collected by filtration
  5. customrecrystallized from methyl cellosolve

出典と根拠

ORDレコード
ord-668a6258d3144e13adb45f39c8f73e07
出典データセット
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04104473

反応ノート

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