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Triethylamine → HCID 39235298, Verbindung

HRID 1984466
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1984466
C(N(CC)CC)C.[OH:8][CH2:9][CH2:10][N:11]1[C:15]([CH3:16])=[CH:14][C:13]([C:17]([NH2:19])=O)=[N:12]1.FC(F)(F)C(OC(=O)C(F)(F)F)=O>ClCCl>[OH:8][CH2:9][CH2:10][N:11]1[C:15]([CH3:16])=[CH:14][C:13]([C:17]#[N:19])=[N:12]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8471Triethylamine2×HCID 9845Trifluoroacetic anhydride2×HCID 669590521-(2-hydroxyethyl)-5-methyl-1H-pyrazole-3-carboxamide

Produkt 1

HCID 39235298HCID 39235298, VerbindungAusbeute 183,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

Under a nitrogen atmosphere, triethylamine (17.9 g, 177 mmol) was added to a slurry of 1-(2-hydroxyethyl)-5-methyl-1H-pyrazole-3-carboxamide (7.0 g, 41.4 mmol) in dichloromethane (70 mL). The mixture was cooled in an ice bath and then a solution of trifluoroacetic anhydride (15.6 g, 74.2 mmol) in dichloromethane (70 mL) was added over a period of 10 minutes. All of the solids dissolved to provide a cloudy solution. After 1 hour additional triethylamine (70.6 mmol) was added and the reaction mixture was cooled in an ice bath. Trifluoroacetic anhydride (35.3 mmol) was added neat over a period of 5 minutes. The reaction mixture was stirred for 10 minutes then the ice bath was removed and the reaction mixture was stirred for 30 minutes. The reaction mixture was diluted with 2 M aqueous sodium carbonate (100 mL) and water (100 mL) then extracted with chloroform (×3). The extracts were combined, dried over magnesium sulfate, filtered, and concentrated under reduced pressure to provide 11.5 g of 1-(2-hydroxyethyl)-5-methyl-1H-pyrazole-3-carbonitrile a brown oil.

Aufarbeitung

  1. temperatureThe mixture was cooled in an ice bath
  2. dissolutionAll of the solids dissolved
  3. customto provide a cloudy solution
  4. temperaturethe reaction mixture was cooled in an ice bath
  5. customthe ice bath was removed
  6. stirringthe reaction mixture was stirred for 30 minutes
  7. additionThe reaction mixture was diluted with 2 M aqueous sodium carbonate (100 mL) and water (100 mL)
  8. extractionthen extracted with chloroform (×3)
  9. dry with materialdried over magnesium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-ffa926481bcf4429b781f830fa92e0ab
Quelldatensatz
uspto-grants-2009_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07544697B2

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