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3-Bromopyridine → 3-Cyclopentylpyridine

HRID 2212078
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2212078
Br[C:2]1[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=1.[CH:8]1([Mg]Cl)[CH2:12][CH2:11][CH2:10][CH2:9]1>O1CCCC1.C1C=CC(P(C2C=CC=CC=2)CCP(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Ni]Cl>[CH:8]1([C:2]2[CH:3]=[N:4][CH:5]=[CH:6][CH:7]=2)[CH2:12][CH2:11][CH2:10][CH2:9]1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 122863-BromopyridineHCID 178478989HCID 178478989, Verbindung2×

Produkt 1

HCID 219638603-CyclopentylpyridineAusbeute 30 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 2734542[1,2-Bis(diphenylphosphino)ethane]dichloronickel(II)KatalysatorHCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
-5 °C

Versuchsvorschrift

3-Bromopyridine (3.9 ml, 40 mmol) and [1,2-bis(diphenylphosphino)ethane]dichloronickel(II) (160 mg, 0.3 mmol) were dissolved in dry tetrahydrofuran (25 ml) and cooled to −5° C. Cyclopentylmagnesium chloride (2.0M in diethyl ether, 20 ml, 40 mmol) was added dropwise over 5–10 minutes and the reaction was allowed to warm slowly to room temperature. Further cyclopentylmagnesium chloride (2.0M in diethyl ether, 5 ml, 10 mmol) was added. The reaction was quenched by the addition of saturated aqueous ammonium chloride solution. The mixture was partitioned between water and ethyl acetate. The organic layer was dried (MgSO4) and concentrated in vacuo. The residue was purified by flash column chromatography on silica, eluting with 20–35% ethyl acetate/i-hexane, to give the title compound (1.74 g, 30%).

Aufarbeitung

  1. temperatureto warm slowly to room temperature
  2. customThe reaction was quenched by the addition of saturated aqueous ammonium chloride solution
  3. customThe mixture was partitioned between water and ethyl acetate
  4. dry with materialThe organic layer was dried (MgSO4)
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by flash column chromatography on silica
  7. washeluting with 20–35% ethyl acetate/i-hexane

Quellen und Nachweise

ORD-Eintrag
ord-27dc71682f4e4c5c9ea1b348d408e5df
Quelldatensatz
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07101892B2

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