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Water → 2-Chloro-3-methyl-1-oxo-1lambda~5~-pyridine

HRID 588370
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 588370
[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N:3]=1.OO.NC(N)=[O:13].FC(F)(F)C(OC(=O)C(F)(F)F)=O.O>C(Cl)Cl>[Cl:1][C:2]1[C:7]([CH3:8])=[CH:6][CH:5]=[CH:4][N+:3]=1[O-:13]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 962WaterHCID 9845Trifluoroacetic anhydrideHCID 31294Carbamide PeroxideHCID 876032-Chloro-3-methylpyridine

Produkt 1

HCID 134316222-Chloro-3-methyl-1-oxo-1lambda~5~-pyridineAusbeute 86 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344
Dichloromethane
Lösungsmittel

Versuchsvorschrift

To a mixture of 2-chloro-3-methylpyridine (15 g, 118 mmol) and urea hydrogen peroxide (44.07 g, 468.5 mmol) in DCM (300 mL) was added trifluoroacetic anhydride (98.55 g, 469.2 mmol) dropwise at 0° C. The mixture was stirred at room temperature for 20 h. The mixture was then poured into water (150 mL), and the layers were separated. The organic layer was washed with saturated aqueous Na2S2O3 (20 mL), dried over Na2SO4, filtered, and the filtrate was concentrated under reduced pressure. The crude product was purified by silica gel flash chromatography (DCM:MeOH, 100:0 to 10:1) to afford the title compound (14.5 g, 86%) as a colorless solid.

Aufarbeitung

  1. customthe layers were separated
  2. washThe organic layer was washed with saturated aqueous Na2S2O3 (20 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationthe filtrate was concentrated under reduced pressure
  6. customThe crude product was purified by silica gel flash chromatography (DCM:MeOH, 100:0 to 10:1)

Quellen und Nachweise

ORD-Eintrag
ord-9b19f3851e914078a67b2c5d960f976f
Quelldatensatz
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09227956B2

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