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Water → 6-Fluoro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile

HRID 392369
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 392369
Cl[C:2]1[N:7]=[C:6]([C:8]#[N:9])[C:5]([S:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[N:4][CH:3]=1.[F-:17].[K+].C(OCC)(=O)C.O>CS(C)=O.[Br-].C([N+](CCCC)(CCCC)CCCC)CCC>[F:17][C:2]1[N:7]=[C:6]([C:8]#[N:9])[C:5]([S:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[N:4][CH:3]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 522689Potassium FluorideHCID 226628046-Chloro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile

Produkt 1

HCID 226628496-Fluoro-3-(phenylsulfanyl)-2-pyrazinecarbonitrileAusbeute 53,6 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 74236
Tetrabutylammonium Bromide
Katalysator
HCID 679Dimethyl SulfoxideLösungsmittel

Reaktionsbedingungen

Temperatur
55 °C

Versuchsvorschrift

In 3.6 mL of dimethyl sulfoxide was dissolved 0.20 g of 6-chloro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile. After adding 0.42 g of potassium fluoride and 0.16 g of tetra-n-butylammonium bromide successively, the mixture thus obtained was stirred at 50-60° C. for 2.5 hours. The reaction mixture was poured into a mixture of 20 mL of ethyl acetate and 20 mL of water, and the organic layer was separated. The organic layer was washed successively with water and saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent: toluene:n-hexane=1:2] to obtain 0.10 g of 6-fluoro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile as a light yellow-colored oily product.

Aufarbeitung

  1. customthe mixture thus obtained
  2. customthe organic layer was separated
  3. washThe organic layer was washed successively with water and saturated aqueous solution of sodium chloride
  4. dry with materialdried on anhydrous magnesium sulfate
  5. customthe solvent was removed under reduced pressure
  6. customThe residue thus obtained
  7. customwas purified by silica gel column chromatography [eluent: toluene:n-hexane=1:2]

Quellen und Nachweise

ORD-Eintrag
ord-4c2f1268c881457ba9eac2091be0501b
Quelldatensatz
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06800629B2

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