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Triphenylphosphine → 2-((Trimethylsilyl)ethynyl)nicotinonitrile

HRID 2197991
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2197991
[CH:1]1[CH:6]=[N:5][C:4](Cl)=[C:3]([C:8]#[N:9])[CH:2]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:29][Si:30]([C:33]#[CH:34])([CH3:32])[CH3:31]>C(N(CC)CC)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:29][Si:30]([CH3:32])([CH3:31])[C:33]#[C:34][C:4]1[N:5]=[CH:6][CH:1]=[CH:2][C:3]=1[C:8]#[N:9]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 11776TriphenylphosphineHCID 66111TrimethylsilylacetyleneHCID 810792-Chloronicotinonitrile

Produkt 1

HCID 134111132-((Trimethylsilyl)ethynyl)nicotinonitrileAusbeute 75 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 167845palladium(II) acetateKatalysator
HCID 8471
Triethylamine
Lösungsmittel

Versuchsvorschrift

In a suitably sized pressure vessel, commercially available 2-chloro-nictinonitrile (1.5 g, 10.8 mmol) was combined with triphenylphosphine (0.228 g, 8 mole %) and palladium (II) acetate (0.083 g, 3.5 mol %) in triethylamine (20 mL). Nitrogen was bubbled through the resulting suspension at room temperature for five minutes then trimethylsilylacetylene (8.5 mL, 60.1 mmol) was added, the vessel sealed and immersed in an 80° C. oil bath. After 18.5 h the pressure tube was cooled to room temperature and the contents were filtered. The filtrate was concentrated under vacuum and the crude product purified by flash chromatography on silica gel eluting with EtOAc/hexanes to give the title compound (1.62 g, 75%) as a tan solid.

Aufarbeitung

  1. customNitrogen was bubbled through the resulting suspension at room temperature for five minutes
  2. customthe vessel sealed
  3. customimmersed in an 80° C.
  4. filtrationthe contents were filtered
  5. concentrationThe filtrate was concentrated under vacuum
  6. customthe crude product purified by flash chromatography on silica gel eluting with EtOAc/hexanes

Quellen und Nachweise

ORD-Eintrag
ord-a4ee9cd44c504768a05dd0feac1534d0
Quelldatensatz
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08338605B2

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