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Sodium Iodide → HCID 178517845, Verbindung

HRID 2106804
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2106804
[I-].[Na+].Cl[Si](C)(C)C.[F:8][C:9]1[C:10]([O:22]C)=[N:11][CH:12]=[C:13]([O:15][C:16]([F:21])([F:20])[CH:17]([F:19])[F:18])[CH:14]=1>C(#N)C.C(Cl)Cl>[F:8][C:9]1[C:10]([OH:22])=[N:11][CH:12]=[C:13]([O:15][C:16]([F:20])([F:21])[CH:17]([F:18])[F:19])[CH:14]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 5238Sodium IodideHCID 6397ChlorotrimethylsilaneHCID 14837013HCID 14837013, Verbindung

Produkt 1

HCID 178517845HCID 178517845, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6342AcetonitrileLösungsmittelHCID 6344Dichloromethane
Lösungsmittel

Versuchsvorschrift

Sodium iodide (1.80 g, 12.0 mmol) and then chlorotrimethylsilane (1.5 ml, 11.8 mmol) were added to a solution of 3-fluoro-2-methoxy-5-(1,1,2,2-tetrafluoroethoxy)pyridine (1.65 g, 6.79 mmol) in 8 ml of acetonitrile with stirring and under nitrogen and the mixture was heated at reflux for 2 5 hours. It was then allowed to cool and was diluted with 20 ml of methylene chloride. The resulting solution was extracted with water and with saturated aqueous sodium hydroxide, dried over sodium sulfate, and concentrated by evaporation under reduced pressure to obtain the title compound as a solid. This was recrystallized from toluene to obtain 0.95 g of the product as a white solid. The proton nmr spectrum was consistent with the assigned structure.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureat reflux for 2 5 hours
  3. temperatureto cool
  4. extractionThe resulting solution was extracted with water and with saturated aqueous sodium hydroxide
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated by evaporation under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-81b3ec38246f49359ea141f79d32f6aa
Quelldatensatz
uspto-grants-1990_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04931452

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