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

HRID 2257141
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HRID 2257141 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 10490579Benzyl 4-(1,2,4-triazol-1-yl)butyrateHCID 178418361HCID 178418361, 화합물

생성물 1

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

시약·촉매·용매 2

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매2회

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-cfd5c3c8255942549ffdd1b1bc8f6354
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05656642

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