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(1-(4-Methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-5-YL)methanol → 1-(4-Methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acid

HRID 610111
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 610111
[F:1][C:2]([F:19])([F:18])[C:3]1[CH:7]=[C:6]([CH2:8][OH:9])[N:5]([C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)[N:4]=1.I([O-])(=O)(=O)=[O:21].[Na+]>C(#N)C.O.[Ru](Cl)(Cl)Cl>[F:19][C:2]([F:1])([F:18])[C:3]1[CH:7]=[C:6]([C:8]([OH:21])=[O:9])[N:5]([C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][CH:11]=2)[N:4]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 2

HCID 11471256(1-(4-Methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-5-YL)methanolHCID 23667635Sodium periodate

Produkt 1

HCID 111619581-(4-Methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazole-5-carboxylic acidAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 61850Ruthenium trichlorideKatalysatorHCID 962Water
Lösungsmittel
HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

To the solution of 3-trifluoromethyl-5-hydroxymethyl-1 -(4-methoxyphenyl)-1H-pyrazole (4.4007 mmol, 1.198 g) in acetonitrile (20 mL) and water (20 mL) was added sodium periodate (1.977, 2.1 eq.) and several crystals of ruthenium(III) chloride at 0° C. This reaction mixture was stirred at ambient temperature for 18 h. The reaction mixture was filtered through Celite to remove white solid impurity and the filter cake washed with 1:1 acetonitrile: water. The filtrate was evaporated in vacuo and the residue was taken up in water. The aqueous was made acidic (pH 3) by the dropwise addition of conc. HCl at 0° C. then extracted with ethyl acetate (3×); the ethyl acetate extracts were washed with brine, dried (MgSO4), and evaporated to gave 1.13 g of pure product (90%).

Aufarbeitung

  1. filtrationThe reaction mixture was filtered through Celite
  2. customto remove white solid impurity
  3. washthe filter cake washed with 1:1 acetonitrile
  4. customThe filtrate was evaporated in vacuo
  5. additionby the dropwise addition of conc. HCl at 0° C.
  6. extractionthen extracted with ethyl acetate (3×)
  7. washthe ethyl acetate extracts were washed with brine
  8. dry with materialdried (MgSO4)
  9. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-4b7e3f39631a4a3198ef325ae94fc6d0
Quelldatensatz
uspto-grants-1999_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05998424

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