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Benzyl 4-(1,2,4-triazol-1-yl)butyrate → 4-(1H-1,2,4-triazol-1-yl)butanoic acid

HRID 962779
ノート
印刷プレビュー

反応式

HRID 962779 の反応式
[N:1]1([CH2:6][CH2:7][CH2:8][C:9]([O:11]CC2C=CC=CC=2)=[O:10])[CH:5]=[N:4][CH:3]=[N:2]1.[H][H]>C(O)C.[C].[Pd]>[N:1]1([CH2:6][CH2:7][CH2:8][C:9]([OH:11])=[O:10])[CH:5]=[N:4][CH:3]=[N:2]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 10490579Benzyl 4-(1,2,4-triazol-1-yl)butyrateHCID 178418361HCID 178418361、化合物

生成物 1

HCID 31574564-(1H-1,2,4-triazol-1-yl)butanoic acid収率 89.1%

試薬・触媒・溶媒 2

HCID 178418390HCID 178418390、化合物触媒HCID 702Ethanol溶媒2 回

実験手順

0.5 g of 5% palladium carbon was added to a solution of 11 g of benzyl 4-(1,2,4-triazol-1-yl)butyrate in 150 ml of ethanol. The mixture was stirred at a hydrogen pressure of 1 atm. at room temperature for 1 hour. Thereto was added 100 ml of ethanol. The mixture was heated and made uniform. Palladium carbon was collected by filtration and washed with ethanol. The filtrate and the washings were combined and concentrated under reduced pressure. To the residue was added a small amount of ethanol. The resulting insolubles were collected by filtration to obtain 6.2 g of 4-(1,2,4-triazol-1-yl)butyric acid as a white powder.

後処理

  1. temperatureThe mixture was heated
  2. filtrationPalladium carbon was collected by filtration
  3. washwashed with ethanol
  4. concentrationconcentrated under reduced pressure
  5. additionTo the residue was added a small amount of ethanol
  6. filtrationThe resulting insolubles were collected by filtration

出典と根拠

ORDレコード
ord-783e429c6fe2487393603243f974a672
出典データセット
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05760058

反応ノート

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