Acetic Acid → 5-(4-cyclopropyl-1H-imidazol-1-yl)-2-fluoro-4-methylbenzonitrile

HRID 402582Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 402582
C(O)(=O)C.OO.[CH:7]1([C:10]2[N:11]=[C:12](S)[N:13]([C:15]3[C:16]([CH3:24])=[CH:17][C:18]([F:23])=[C:19]([CH:22]=3)[C:20]#[N:21])[CH:14]=2)[CH2:9][CH2:8]1.S([O-])([O-])=O.[Na+].[Na+]>O>[CH:7]1([C:10]2[N:11]=[CH:12][N:13]([C:15]3[C:16]([CH3:24])=[CH:17][C:18]([F:23])=[C:19]([CH:22]=3)[C:20]#[N:21])[CH:14]=2)[CH2:8][CH2:9]1

Komponenten

6

Edukt 4

HCID 176Acetic AcidHCID 784Hydrogen PeroxideHCID 24437Sodium SulfiteHCID 178427859HCID 178427859, Verbindung

Produkt 1

HCID 866912495-(4-cyclopropyl-1H-imidazol-1-yl)-2-fluoro-4-methylbenzonitrile

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel2×

Reaktionsbedingungen

Temperatur
45 °C

Versuchsvorschrift

In a 500 mL three neck round bottom flask was placed acetic acid (96 mL), water (19 mL) and hydrogen peroxide (30%, 7.47 mL, 65.88 mmol). The mixture was heated to 45° C. with stirring under nitrogen while monitoring the internal temperature. 5-(4-Cyclopropyl-2-mercapto-1H-imidazol-1-yl)-2-fluoro-4-methylbenzonitrile (6.00 g, 21.96 mmol) was then added as a solid in small portions over 30 minutes while maintaining an internal temperature below 55° C. When addition of the thioimidazole was complete the reaction was stirred for 30 minutes at a temperature of 45° C., and then cooled to room temperature, and a solution of 20% wt/wt sodium sulfite in water (6 mL) was slowly added. The mixture was stirred for 30 minutes and solvents were removed under reduced pressure. The residue was suspended in 250 mL of water and 4N aqueous ammonium hydroxide was added to bring the pH to ˜10. The mixture was extracted with dichloromethane (3×200 ml), the organics combined, dried over magnesium sulfate, and the solvent was removed under reduced pressure. The residue was dissolved in 20 mL EA, and 80 mL of hexanes were added with stirring. The solvents were decanted off and an oily residue was left behind. This process was repeated and the product, 5-(4-cyclopropyl-1H-imidazol-1-yl)-2-fluoro-4-methylbenzonitrile was obtained as a viscous oil (5.14 g, 21.33 mmol) Anal. LC/MS (m/z: 242, M+1)

Aufarbeitung

  1. temperaturewhile maintaining an internal temperature below 55° C
  2. stirringwas stirred for 30 minutes at a temperature of 45° C.
  3. temperaturecooled to room temperature
  4. stirringThe mixture was stirred for 30 minutes
  5. customsolvents were removed under reduced pressure
  6. addition4N aqueous ammonium hydroxide was added
  7. extractionThe mixture was extracted with dichloromethane (3×200 ml)
  8. dry with materialdried over magnesium sulfate
  9. customthe solvent was removed under reduced pressure
  10. dissolutionThe residue was dissolved in 20 mL EA
  11. addition80 mL of hexanes were added
  12. stirringwith stirring
  13. customThe solvents were decanted off
  14. waitan oily residue was left behind

Quellen und Nachweise

ORD-Eintrag
ord-cd59bb84783c400c8767bad8b036e67b
Quelldatensatz
uspto-grants-2014_06
Patentnummer
US08742126B2

Notizen zur Reaktion

Wird geladen…