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1H,1H,2H,2H-Perfluorooctyldimethylchlorosilane → HCID 86663263, Verbindung

HRID 1408492
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1408492
[F:1][C:2]([F:25])([C:9]([F:24])([F:23])[C:10]([F:22])([F:21])[C:11]([F:20])([F:19])[C:12]([F:18])([F:17])[C:13]([F:16])([F:15])[F:14])[CH2:3][CH2:4][Si:5]([CH3:8])([CH3:7])Cl.[C:26]([Mg]Br)#[CH:27]>C1COCC1>[F:1][C:2]([F:25])([C:9]([F:24])([F:23])[C:10]([F:22])([F:21])[C:11]([F:20])([F:19])[C:12]([F:18])([F:17])[C:13]([F:16])([F:15])[F:14])[CH2:3][CH2:4][Si:5]([C:26]#[CH:27])([CH3:8])[CH3:7]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 1453821H,1H,2H,2H-PerfluorooctyldimethylchlorosilaneHCID 178418486HCID 178418486, Verbindung

Produkt 1

HCID 86663263HCID 86663263, VerbindungAusbeute 96 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

In an oven-dried 250-mL round bottom flask, 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyldimethylchlorosilane (9.67 g, 21.9 mmol) was dissolved in 20 mL anhydrous THF. Ethynylmagnesium bromide (50 mL, 25 mmol, 0.5 M in THF) was added and the mixture was heated to 60° C. for 12 hr. After allowing the mixture to cool to room temperature, the reaction was quenched by the dropwise addition of water, followed by the addition of dilute sulfuric acid to dissolve the magnesium salts. The organic layer was separated, washed with water (3×20 mL) and brine, dried over magnesium sulfate, filtered and concentrated under vacuum. The crude product was purified by chromatography on silica gel using hexane as an eluant. Removal of solvent yielded 9.0 g (21 mmol, 96%) of the product as a colorless liquid. Analysis of the colorless product provided the following data: 1H-NMR (200 MHz, CDCl3) δ=2.4 (s, 1H), 2.1 (m, 2H), 0.8 (m, 2H), 0.2 (s, 6H).

Aufarbeitung

  1. temperatureto cool to room temperature
  2. customthe reaction was quenched by the dropwise addition of water
  3. additionfollowed by the addition of dilute sulfuric acid
  4. dissolutionto dissolve the magnesium salts
  5. customThe organic layer was separated
  6. washwashed with water (3×20 mL) and brine
  7. dry with materialdried over magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under vacuum
  10. customThe crude product was purified by chromatography on silica gel
  11. customRemoval of solvent

Quellen und Nachweise

ORD-Eintrag
ord-84dc760a22074a3cb7c86cf1c2fbcbc4
Quelldatensatz
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08920679B2

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