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Methane → 1-(4-Fluorophenyl)-1H-imidazole-4-carboxylic acid

HRID 447214
ノート
印刷プレビュー

反応式

HRID 447214 の反応式
C([O:3][C:4]([C:6]1[N:7]=[CH:8][N:9]([C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[CH:10]=1)=[O:5])C.C>O1CCOCC1.[OH-].[Na+]>[F:17][C:14]1[CH:13]=[CH:12][C:11]([N:9]2[CH:10]=[C:6]([C:4]([OH:5])=[O:3])[N:7]=[CH:8]2)=[CH:16][CH:15]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 297MethaneHCID 17390092HCID 17390092、化合物

生成物 1

HCID 173900481-(4-Fluorophenyl)-1H-imidazole-4-carboxylic acid

試薬・触媒・溶媒 2

HCID 14798Sodium Hydroxide溶媒HCID 312751,4-Dioxane溶媒

実験手順

Crude 1-(4-fluoro-phenyl)-1H-imidazole-4-carboxylic acid ethyl ester (175 mmol) was dissolved in 450 mL dioxane and 450 mL 2N sodium hydroxide solution. The reaction mixture was refluxed for 2 h. Charcoal (1 g, Norit SA II) was added and reflux was continued for another 20 min. The mixture was filtered hot and washed with 50 mL 2N sodium hydroxide solution. The filtrate was treated with 550 mL 2N HCl and stirred at room temperature overnight. The solid material was filtered off and dried at 50° C. and 15 mbar. The desired compound was obtained as an off-white solid (28 g, 78%), MS: m/e 205.1 (M−H).

後処理

  1. temperatureThe reaction mixture was refluxed for 2 h
  2. temperaturereflux
  3. filtrationThe mixture was filtered hot
  4. washwashed with 50 mL 2N sodium hydroxide solution
  5. additionThe filtrate was treated with 550 mL 2N HCl
  6. filtrationThe solid material was filtered off
  7. customdried at 50° C.

出典と根拠

ORDレコード
ord-bd06e6e942904a0bafdcaa2420f5e1be
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08481548B2

反応ノート

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