4-Fluorophenol → 2-(4-Fluorophenoxymethyl)-3-nitropyridine

HRID 1445001Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1445001
Br[CH2:2][C:3]1[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][CH:6]=[CH:5][N:4]=1.[F:12][C:13]1[CH:18]=[CH:17][C:16]([OH:19])=[CH:15][CH:14]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O.C(OCC)(=O)C>[F:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][CH2:2][C:3]2[C:8]([N+:9]([O-:11])=[O:10])=[CH:7][CH:6]=[CH:5][N:4]=2)=[CH:15][CH:14]=1

Komponenten

6

Edukt 3

HCID 97324-FluorophenolHCID 11430Potassium CarbonateHCID 218311782-(Bromomethyl)-3-nitropyridine

Produkt 1

HCID 671428762-(4-Fluorophenoxymethyl)-3-nitropyridineAusbeute 62,7 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228DimethylformamideLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

2-Bromomethyl-3-nitropyridine (100 mg, 0.456 mmol) prepared in Step 2 was added at room temperature to a solution of 4-fluorophenol (56 mg, 0.502 mmol) and potassium carbonate (189 mg, 1.37 mmol) in N,N-dimethylformamide (3 ml) and then stirred for 3 hours. The reaction mixture was diluted with ethyl acetate (10 ml), washed with a saturated sodium bicarbonate solution, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography (dichloromethane/n-hexane=2/1, v/v) to give 71 mg of the titled compound as yellow solid.

Aufarbeitung

  1. washwashed with a saturated sodium bicarbonate solution
  2. dry with materialdried on anhydrous magnesium sulfate
  3. concentrationconcentrated under reduced pressure
  4. customThe resulting residue was purified with silica gel column chromatography (dichloromethane/n-hexane=2/1, v/v)

Quellen und Nachweise

ORD-Eintrag
ord-43c8db83c99c42f8a51f8df23e755fdb
Quelldatensatz
uspto-grants-2010_02
Patentnummer
US07662832B2

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