Hydrochloric Acid → 1-benzyl-5-methyl-1H-imidazole-4-carboxylic acid

HRID 1428985ノート

反応式

HRID 1428985 の反応式
[CH2:1]([N:8]1[C:12]([CH3:13])=[C:11]([C:14]([O:16]CC)=[O:15])[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[K+].Cl>CO>[CH2:1]([N:8]1[C:12]([CH3:13])=[C:11]([C:14]([OH:16])=[O:15])[N:10]=[CH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 13896233ethyl 1-benzyl-5-methyl-1H-imidazole-4-carboxylate

生成物 1

HCID 538968611-benzyl-5-methyl-1H-imidazole-4-carboxylic acid収率 91%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
80 °C

実験手順

Part A: To a magnetically stirred solution of ethyl N-benzyl-5-methyl-1H-imidazole-4-carboxylate (8.4 gram, 0.0345 mol) in methanol (200 ml) was slowly added a solution of KOH (7.3 gram, 85% grade, 0.110 mol) and the resulting mixture was heated at 80° C. for 2 hours. The solution was cooled to room temperature and concentrated HCl (9.2 ml) was subsequently added. The formed precipitate was collected by filtration to give N-benzyl-5-methyl-1H-imidazole-4-carboxylic acid (6.77 gram, 91% yield). Melting point: 292° C. (decomposition).

後処理

  1. temperatureThe solution was cooled to room temperature
  2. filtrationThe formed precipitate was collected by filtration

出典と根拠

ORDレコード
ord-e8ceffc561df494b95e80787f3aff0af
出典データセット
uspto-grants-2015_01
特許番号
US08937184B2

反応ノート

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