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Sodium Iodide → HCID 178517851, Verbindung

HRID 1623239
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1623239
[F:1][C:2]1[C:3]([O:9]C)=[N:4][C:5]([F:8])=[CH:6][CH:7]=1.[I-].[Na+].Cl[Si](C)(C)C>C(#N)C.CCOC(C)=O.O>[F:1][C:2]1[C:3]([OH:9])=[N:4][C:5]([F:8])=[CH:6][CH:7]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 3

HCID 5238Sodium IodideHCID 6397ChlorotrimethylsilaneHCID 669368673,6-Difluoro-2-methoxypyridine

Produkt 1

HCID 178517851HCID 178517851, VerbindungAusbeute 55,7 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 6342
Acetonitrile
Lösungsmittel
HCID 8857Ethyl AcetateLösungsmittel

Reaktionsbedingungen

Temperatur
82.5 °C

Versuchsvorschrift

To 3,6-difluoro-2-methoxypyridine (21.5 g, 148 mmol) in acetonitrile (250 ml) was added sodium iodide (66.6 g, 445 mmol) and chlorotrimethylsilane (56.8 ml, 445 mmol). The resulting mixture was heated at 80-85° C. for 2.5 hr. The mixture was cooled to ambient temperature and diluted with EtOAc (300 mL) and water (300 mL) and vigorously stirred for another hr. The layers were separated, and the aqueous phase was extracted with additional ethyl acetate (200 mL). The combined organic layers were washed sequentially with 0.6 N aqueous HCl (250 mL) and brine (250 mL) and concentrated in vacuo to yield a slurry. The slurry was filtered and rinsed three times with cold acetonitrile to yield 10.8 g of desired product as a white solid. The filtrate was concentrated and purified by flash chromatography over silica gel (heptanes:ethyl acetate gradient) to give an additional 4.2 g (77% yield combined) of 3,6-difluoro-2-hydroxypyridine as a white solid. LCMS (m/z): 132.0 [M+H]+; retention time=0.47 min.

Aufarbeitung

  1. temperatureThe mixture was cooled to ambient temperature
  2. customThe layers were separated
  3. extractionthe aqueous phase was extracted with additional ethyl acetate (200 mL)
  4. washThe combined organic layers were washed sequentially with 0.6 N aqueous HCl (250 mL) and brine (250 mL)
  5. concentrationconcentrated in vacuo
  6. customto yield a slurry
  7. filtrationThe slurry was filtered
  8. washrinsed three times with cold acetonitrile

Quellen und Nachweise

ORD-Eintrag
ord-949821bf009f40ba941c5c8de8100d9c
Quelldatensatz
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08778951B2

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