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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
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 962779
[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
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Komponenten

5

Edukt 2

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

Produkt 1

HCID 31574564-(1H-1,2,4-triazol-1-yl)butanoic acidAusbeute 89,1 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 178418390HCID 178418390, VerbindungKatalysatorHCID 702EthanolLösungsmittel2×

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-783e429c6fe2487393603243f974a672
Quelldatensatz
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05760058

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