Hydrochloric Acid → 3-(Difluoromethyl)-1-methyl-4,5-dihydro-1H-pyrazole-4-carboxylic acid

HRID 1674486Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1674486
C([O:3][C:4]([CH:6]1[CH2:10][N:9]([CH3:11])[N:8]=[C:7]1[CH:12]([F:14])[F:13])=[O:5])C.[OH-].[Na+].Cl>O1CCOCC1>[F:14][CH:12]([F:13])[C:7]1[CH:6]([C:4]([OH:5])=[O:3])[CH2:10][N:9]([CH3:11])[N:8]=1

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 67338397HCID 67338397, Verbindung

Produkt 1

HCID 673384023-(Difluoromethyl)-1-methyl-4,5-dihydro-1H-pyrazole-4-carboxylic acid

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

3-Difluoromethyl-1-methyl-4,5-dihydro-1H-pyrazole-4-carboxylic acid ethyl ester (0.15 g, 0.7 mmol) was dissolved in 2 ml of dioxan. 1.5 ml of a 1 N aqueous sodium hydroxide solution (1.5 mmol) were added and the reaction mixture was stirred for 2 h at room temperature. Subsequently the mixture was acidified with concentrated hydrochloric acid (pH 2). The dioxan was removed in vacuo, the residue was extracted with ethyl acetate. The combined organic layer was washed with brine, dried over magnesium sulfate and evaporated, delivering 0.1 g of 3-difluoromethyl-1-methyl-4,5-dihydro-1H-pyrazole-4-carboxylic acid, which could be directly used in the next step without further purification.

Aufarbeitung

  1. customThe dioxan was removed in vacuo
  2. extractionthe residue was extracted with ethyl acetate
  3. washThe combined organic layer was washed with brine
  4. dry with materialdried over magnesium sulfate
  5. customevaporated
  6. customcould be directly used in the next step without further purification

Quellen und Nachweise

ORD-Eintrag
ord-023bbf28d75a4b4eb829840f5435e97c
Quelldatensatz
uspto-grants-2011_08
Patentnummer
US08003626B2

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