Dimethylformamide → 2-Fluoro-6-(2-trifluoromethyl-4-thienyloxy)pyridine

HRID 1348994

Reaktionsgleichung

Reaktionsgleichung von HRID 1348994
F[C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[N:3]=1.CN(C=O)C.C([O-])([O-])=O.[K+].[K+].[OH:20][C:21]1[CH:22]=[C:23]([C:26]([F:29])([F:28])[F:27])[S:24][CH:25]=1>O>[F:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([O:20][C:21]2[CH:22]=[C:23]([C:26]([F:29])([F:28])[F:27])[S:24][CH:25]=2)[N:3]=1

Komponenten

6

Edukt 4

HCID 6228DimethylformamideHCID 11430Potassium CarbonateHCID 739342,6-DifluoropyridineHCID 110842734-Hydroxy-2-(trifluoromethyl)thiophene

Produkt 1

HCID 121159912-Fluoro-6-(2-trifluoromethyl-4-thienyloxy)pyridineAusbeute 74,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

1.00 g of 2,6-difluoropyridine is introduced into 10 ml of DMF under nitrogen and 1.44 g of K2CO3 are added at RT. 1.61 g of 4-hydroxy-2-trifluoromethylthiophene are added and the mixture is heated at 80° C. for 4 h, then cooled to RT and poured into water. After extraction twice with heptane/ethyl acetate (1:1) and twice with ethyl acetate the product is washed with water and saturated sodium chloride solution, dried over MgSO4 and concentrated. Chromatographic purification on silica gel with heptane/ethyl acetate (3:7) as eluent gives 1.7 g of 2-fluoro-6-(2-trifluoromethyl-4-thienyloxy)pyridine as a colorless oil.

Aufarbeitung

  1. temperaturecooled to RT
  2. extractionAfter extraction twice with heptane/ethyl acetate (1:1)
  3. washtwice with ethyl acetate the product is washed with water and saturated sodium chloride solution
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. customChromatographic purification on silica gel with heptane/ethyl acetate (3:7) as eluent

Quellen und Nachweise

ORD-Eintrag
ord-9169015d135343b7bf4f71314f831d37
Quelldatensatz
uspto-grants-2007_05
Patentnummer
US07211673B2

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