Acetic Acid → 1H-Pyrazole-5-carboxylic acid, 1-methyl-3-propyl-, ethyl ester

HRID 354163Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 354163
[C:1]([O:8][CH2:9][CH3:10])(=[O:7])[C:2](OCC)=O.[CH3:11][C:12](=O)[CH2:13][CH2:14][CH3:15].[Na].C(O)(=O)C.[CH3:22][NH:23][NH2:24]>C(O)C>[CH3:22][N:23]1[C:2]([C:1]([O:8][CH2:9][CH3:10])=[O:7])=[CH:11][C:12]([CH2:13][CH2:14][CH3:15])=[N:24]1

Komponenten

7

Edukt 5

HCID 176Acetic AcidHCID 6061MethylhydrazineHCID 7268Diethyl OxalateHCID 78952-PentanoneHCID 5360545Sodium

Produkt 1

HCID 101765321H-Pyrazole-5-carboxylic acid, 1-methyl-3-propyl-, ethyl esterAusbeute 15,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

A solution of diethyl oxalate (27.2 mL, 0.2 mol) in 2-pentanone (21.2 mL, 0.2 mol) was added dropwise to a solution of sodium (4.83 g, 0.21 mol) in ethanol (200 mL), and the reaction stirred at 60° C. for 5 h, then cooled in an ice-bath. The solution was neutralised using acetic acid (11.5 mL, 0.2 mol) and N-methyl hydrazine (10.6 mL, 0.2 mol) then added dropwise. The mixture was stirred for a further 4 h at room temperature and concentrated under reduced pressure. The residue was partitioned between dichloromethane (300 mL) and water (200 mL), and the phases separated. The aqueous layer was extracted with dichloromethane (3×100 mL), the combined organic solutions were dried (MgSO4) and evaporated under reduced pressure. The crude product was purified by column chromatography on silica gel, using ethyl acetate:hexane (25:75) as eluant to give ethyl 1-methyl-3-n-propyl-pyrazole-5-carboxylate (6.1 g) and the title compound (22.1 g, 56%).

Aufarbeitung

  1. temperaturecooled in an ice-bath
  2. additionthen added dropwise
  3. stirringThe mixture was stirred for a further 4 h at room temperature
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was partitioned between dichloromethane (300 mL) and water (200 mL)
  6. customthe phases separated
  7. extractionThe aqueous layer was extracted with dichloromethane (3×100 mL)
  8. dry with materialthe combined organic solutions were dried (MgSO4)
  9. customevaporated under reduced pressure
  10. customThe crude product was purified by column chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-459b05afdf3b4fb5887d1c7b77447c8f
Quelldatensatz
uspto-grants-2004_06
Patentnummer
US06756373B1

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