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Hydrogen Peroxide → (3,3,4,4,4-Pentafluorobutylsulfonyl)acetonitrile

HRID 888640
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 888640
[F:1][C:2]([F:13])([C:9]([F:12])([F:11])[F:10])[CH2:3][CH2:4][S:5][CH2:6][C:7]#[N:8].OO.S([O-])([O-])=[O:17].[Na+].[Na+].[OH2:22]>O.O.[O-][W]([O-])(=O)=O.[Na+].[Na+]>[F:13][C:2]([F:1])([C:9]([F:10])([F:11])[F:12])[CH2:3][CH2:4][S:5]([CH2:6][C:7]#[N:8])(=[O:17])=[O:22]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 784Hydrogen Peroxide2×HCID 962WaterHCID 24437Sodium SulfiteHCID 86642963(3,3,4,4,4-Pentafluorobutylthio)acetonitrile

Produkt 1

HCID 57425691(3,3,4,4,4-Pentafluorobutylsulfonyl)acetonitrile

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 150191
Sodium Tungstate Dihydrate
Katalysator

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

To a suspension of 17.81 g of (3,3,4,4,4-pentafluorobutylthio)acetonitrile and 0.28 g of sodium tungstate dihydrate in 30 ml of water was added 8.94 ml of 31% aqueous hydrogen peroxide while the suspension was stirred. The temperature of the mixture was raised to 65° C., and 8.94 ml of 31% aqueous hydrogen peroxide was added thereto. The mixture was stirred at 70° C. for 1 hour. In the middle of the reaction, the formation of a deduced sulfoxide compound was confirmed by thin layer chromatography (TLC) analysis. The reaction mixture was cooled to room temperature, and 30 ml of an aqueous sodium sulfite solution was added thereto, followed by extraction with 150 ml of ethyl acetate three times. Organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried over sodium sulfate, filtered, and then concentrated under reduced pressure. The residue was crystallized from chloroform:hexane=1:2 to obtain 17.84 g of (3,3,4,4,4-pentafluorobutylsulfonyl)acetonitrile represented by the formula:

Aufarbeitung

  1. stirringThe mixture was stirred at 70° C. for 1 hour
  2. customIn the middle of the reaction
  3. temperatureThe reaction mixture was cooled to room temperature
  4. extractionfollowed by extraction with 150 ml of ethyl acetate three times
  5. washwashed with an aqueous saturated sodium chloride solution
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was crystallized from chloroform

Quellen und Nachweise

ORD-Eintrag
ord-091d3e06be1d40689933f93d3be23022
Quelldatensatz
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08247596B2

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