Reaktion #75899

ord-5a38d8ca83fe481f95fcda3c99627090

Reaktionsgleichung

O
Water
CCn1nc(C)c(C(=O)c2ccccc2)c1Cl
(5-chloro-1-ethyl-3-methyl-1H-pyrazol-4-yl)-phenyl-methanone
COc1ccc(O)cc1
4-methoxyphenol
[H-].[Na+]
sodium hydride
CCn1nc(C)c(C(=O)c2ccccc2)c1Oc1ccc(OC)cc1
[1-ethyl-5-(4-methoxyphenoxy)-3-methyl-1H-pyrazol-4-yl]-phenyl-methanone
Ausbeute 57.3%

Lösungsmittel

Reaktionsbedingungen

Temperatur
110°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe mixture was extracted three times with 10 ml of dichloromethane
  2. 2
    TrocknenThe combined extracts were dried over magnesium sulphate
  3. 3
    Filtrationfiltered
  4. 4
    Sonstigeevaporated
  5. 5
    SonstigeThe residue was purified by flash chromatography on silica gel
  6. 6
    Waschenfor the elution

Vorschrift

A mixture of 129 mg of (5-chloro-1-ethyl-3-methyl-1H-pyrazol-4-yl)-phenyl-methanone, 141 mg of 4-methoxyphenol and 33 mg of sodium hydride (60% in mineral oil) in 3 ml of anhydrous N,N-dimethylformamide was stirred under nitrogen at 110° C. for 5 h. Water (8 ml) was added and the mixture was extracted three times with 10 ml of dichloromethane. The combined extracts were dried over magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using ethyl acetate/petroleum ether (bp 40-60° C.) (1:3) for the elution to give 100 mg of [1-ethyl-5-(4-methoxyphenoxy)-3-methyl-1H-pyrazol-4-yl]-phenyl-methanone as a yellow oil. Mass spectrum (ES) m/z 337 [M]+, 378 [M+H+CH3CN]+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06699887B2uspto-grants-2004_03